US5886011A - Piperidine derivatives as substance P antagonists - Google Patents

Piperidine derivatives as substance P antagonists Download PDF

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Publication number
US5886011A
US5886011A US08/913,824 US91382497A US5886011A US 5886011 A US5886011 A US 5886011A US 91382497 A US91382497 A US 91382497A US 5886011 A US5886011 A US 5886011A
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methyl
amino
dihydrobenzofuran
pharmaceutically acceptable
phenylpiperidine hydrochloride
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US08/913,824
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Yoshihiro Tanoue
Koichi Beppu
Akira Okayama
Osami Sakamoto
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Hisamitsu Pharmaceutical Co Inc
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Hisamitsu Pharmaceutical Co Inc
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Assigned to HISAMITSU PHARMACEUTICAL CO., INC. reassignment HISAMITSU PHARMACEUTICAL CO., INC. ASSIGNMENT OF ASSIGNORS INTEREST (SEE DOCUMENT FOR DETAILS). Assignors: BEPPU, KOICHI, OKAYAMA, AKIRA, SAKAMOTO, OSAMI, TANOUE, YOSHIHIRO
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    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D405/00—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom
    • C07D405/02—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing two hetero rings
    • C07D405/12—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing two hetero rings linked by a chain containing hetero atoms as chain links
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00—Medicinal preparations containing organic active ingredients
    • A61K31/33—Heterocyclic compounds
    • A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/435—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom
    • A61K31/44—Non condensed pyridines; Hydrogenated derivatives thereof
    • A61K31/445—Non condensed piperidines, e.g. piperocaine
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P1/00—Drugs for disorders of the alimentary tract or the digestive system
    • A61P1/08—Drugs for disorders of the alimentary tract or the digestive system for nausea, cinetosis or vertigo; Antiemetics
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P11/00—Drugs for disorders of the respiratory system
    • A61P11/06—Antiasthmatics

Definitions

  • the present invention relates to new piperidine derivatives having an antagonism on Substance P, being a peptide neurotransmitter, and pharmaceutically acceptable acid addition salts thereof.
  • the piperidine derivatives and pharmaceutically acceptable acid addition salts thereof of the present invention are useful as a preventive or remedy for respiratory system diseases, central nervous system diseases, digestive system diseases, circulatory system diseases, and a variety of inflammation and pains and the like.
  • Substance P is a tachykinin undecapeptide which is found especially in mammals and which is referred as Neurokinin with Neurokinin A and Neurokinin B etc.
  • the facts that Substance P is involved in a variety of pathological fields such as respiratory system diseases such as asthma, central nervous system diseases such as anxiety, schizophrenia, digestive system diseases such as ulcerative colitis, circulatory system diseases such as hypertension, various inflammation and pains, have been well-known (e.g., Journal of Medicinal Chemistry,25,1009, (1982), Trends in Cluster Headache, 85-97, (1987),ELSEVIER).
  • non-peptide Substance P antagonist a compound having a quinuclidine skeleton (JP 3-503768, A), a compound having a piperidine skeleton (JP 4-103570, A), a compound having an isoindolone skeleton (JP 3-176469, A), a compound having an arylalkylamine skeleton (JP 3-206086, A) etc. have been known.
  • the object of the present invention is to provide piperidine derivatives or pharmaceutically acceptable acid addition salts thereof having an antagonism on non-peptide Substance P.
  • the present invention provides piperidine derivatives represented by general formula (I) ##STR2## or pharmaceutically acceptable acid addition salts thereof: wherein n represents an integer of 0 or 1; X represents CH 2 , O or CH--CH 3 ; R represents hydrogen, halogen, lower alkyl, hydroxy, lower alkoxy, lower alkylthio, lower alkylsulfinyl, lower alkylsulfonyl, substituted aminosulfonyl or nitro; R 1 and R 2 may be the same or different and each represents hydrogen or lower alkyl.
  • general formula (I) ##STR2## or pharmaceutically acceptable acid addition salts thereof: wherein n represents an integer of 0 or 1; X represents CH 2 , O or CH--CH 3 ; R represents hydrogen, halogen, lower alkyl, hydroxy, lower alkoxy, lower alkylthio, lower alkylsulfinyl, lower alkylsulfonyl, substituted aminosulfonyl
  • the present invention also provides cis-piperidine derivatives represented by general formula (Ia) ##STR3## or pharmaceutically acceptable acid addition salts thereof: wherein n, X, R, R 1 and R 2 are as defined above.
  • the present invention also provides cis-piperidine derivatives represented by general formula (Ib) ##STR4## or pharmaceutically acceptable acid addition salts thereof: wherein R, R 1 and R 2 are as defined above.
  • the present invention also provides the piperidine derivatives or pharmaceutically acceptable acid addition salts thereof having an antagonism on Substance P.
  • the present invention also provides a pharmaceutical composition
  • a pharmaceutical composition comprising an effective amount of the piperidine derivative or pharmaceutically acceptable acid addition salt thereof, and a pharmaceutically acceptable carrier.
  • the present invention also provides a preventive or remedy for asthma which comprises the piperidine derivative or pharmaceutically acceptable acid addition salt thereof as an effective component.
  • the present invention also provides a preventive or remedy for vomiting which comprises the piperidine derivative or pharmaceutically acceptable acid addition salt thereof as an effective component.
  • the present invention also provides a formulation for oral administration, a formulation for parenteral administration, a formulation for intrarectal administration or a formulation for percutaneous administration which comprises the piperidine derivative or pharmaceutically acceptable acid addition salt thereof as an effective component.
  • n represents an integer of 0 or 1.
  • n a form of condensed five-membered ring with benzen ring is shown.
  • n 1, a form of condensed six-membered ring with benzen ring is shown.
  • X represents CH 2 , O or CH--CH 3 substituted by a methyl group from methylene group in the ring.
  • R represents a substituent group on the phenyl group in the condensed ring, including non-substituted condition.
  • R represents hydrogen, halogen, lower alkyl, hydroxy, lower alkoxy, lower alkylthio, lower alkylsulfinyl, lower alkylsulfonyl, substituted aminosulfonyl or nitro.
  • halogen means fluorine, chlorine, bromine or iodine.
  • the lower alkyl group represents a cyclic or acyclic alkyl group having C 1-6 which may contain one to five halogen such as fluorine in any position.
  • halogen such as fluorine in any position.
  • methyl, ethyl, n-propyl, iso-propyl, n-butyl, iso-butyl, tert-butyl, n-pentyl, n-hexyl, cyclopentyl, cyclohexyl, monofluoromethyl, difluoromethyl, trifluoromethyl, trifluoro-ethyl and perfluoroethyl may be exemplified.
  • the lower alkoxy group represents a cyclic or acyclic alkoxy group having C 1-6 which may contain one to five halogen such as fluorine in any position.
  • methoxy, ethoxy, n-propoxy, iso-propoxy, n-butoxy, iso-butoxy, tert-butoxy, n-pentyloxy, n-hexyloxy, cyclopentyloxy, cyclohexyloxy, monofluoromethoxy, difluoromethoxy, trifluoromethoxy, trifluoroethoxy and perfluoroetyoxy may be exemplified.
  • the lower alkylthio group represents a cyclic or acyclic alkylthio group having C 1-6 which may contain one to five halogen atoms such as fluorine in any position.
  • halogen atoms such as fluorine in any position.
  • the lower alkylsulfinyl group represents a cyclic or acyclic alkylsulfinyl group having C 1-6 which may contain one to five halogen atoms such as fluorine in any position.
  • the lower alkylsulfinyl group methylsulfinyl, ethylsulfinyl, n-propylsulfinyl, iso-propylsulfinyl, n-butylsulfinyl, iso-butylsulfinyl, tert-butylsulfinyl, n-pentylsulfinyl, n-hexylsulfinyl, cyclopentylsulfinyl, cyclohexylsulfonyl, monofluoromethylsulfinyl, difluoromethylsulfinyl, trifluoromethylsulfinyl, trifluoro
  • the lower alkylsulfonyl group represents a cyclic or acyclic alkylsulfonyl group having C 1-6 which may contain one to five halogen atoms such as fluorine in any position.
  • halogen atoms such as fluorine in any position.
  • the substituted aminosulfonyl group represents a cyclic or acyclic alkylaminosulfonyl group having C 1-6 which may contain one to five halogen atoms such as fluorine in any position, and represents an aminosulfonyl group in which an amino group forms a part of the cyclic compound.
  • substituted aminosulfonyl group methylaminosulfonyl, ethylaminosulfonyl, n-propylaminosulfonyl, iso-propylaminosulfonyl, n-butylaminosulfonyl, iso-butylaminosulfonyl, tert-butylaminosulfonyl, n-pentylaminosulfonyl, n-hexylaminosulfonyl, dimethylaminosulfonyl, diethylaminosulfonyl, di-n-propylaminosulfonyl, diisopropylaminosulfonyl, di-n-butylaminosulfonyl, diisobutylaminosulfonyl, cyclopentylaminosulfonyl, cyclohexylaminosulfonyl, monofluoromethylaminosulf
  • R 1 and R 2 may be the same or different and each represents hydrogen or a lower alkyl.
  • the lower alkyl group methyl, ethyl, n-propyl, isopropyl, n-butyl, isobutyl may be exemplified.
  • the forms of unsubstitution, monoalkyl and dialkyl may be made.
  • the present invention includes any forms of stereoisomers produced in monoalkyl, diastereomer and mixtures thereof.
  • the present invention includes both of cis-isomer and trans-isomer of the compound (I), among which cis-isomer represented by the formula (Ia) is most preferable.
  • salts formed with an inorganic acid such as hydrochloric acid, hydrobromic acid, sulfuric acid, nitric acid, phosphoric acid: or salts formed with an organic acid such as acetic acid, propionic acid, glycolic acid, lactic acid, malic acid, tartaric acid, citric acid, ascorbic acid, maleic acid, oxalic acid, fumaric acid, succinic acid, malonic acid, methanesulfonic acid, benzensulfonic acid, toluene-sulfonic acid, may be exemplified.
  • the acid addition salts are, however, not limited by the examples.
  • (2S,3S)-3- (5-trifluoromethoxy-2,3-dihydrobenzofuran-7-yl)methyl!amino-2-phenylpiperidine hydrochloride may be exemplified.
  • the piperidine derivatives and pharmaceutically acceptable acid addition salts thereof of the present invention are useful as a preventive or remedy for respiratory system diseases, central nervous system diseases, digestive system diseases, circulatory system diseases, and a variety of inflammation and pains and the like.
  • these diseases and inflammations chronic bronchial obstruction, asthma, migraine, vomiting, anxiety, depression, melancholia, Alzheimer's diseases, dementia, stomatosis caused by stress, anaphylaxis, colitis, hypertension, vasospamic diseases, hidebound disease, arthritis, psoriasis, rheumatic diseases, multiple sclerosis, systemic lupus erythematosus, initis, drug toxicosis may be exemplified.
  • the compound represented by the general formula (I), (Ia) or (Ib) or the pharmaceutically acceptable acid addition salt thereof is administered as a drug, it may be administered as it is, or it may be made into any forms of formulations for oral administration, parenteral administration, intrarectal administration and percutaneous administration together with known carriers.
  • the formulation for oral administration is not limited to, but solid or liquid formulations such as powdered drug, powders, capsules, granules, tablets, syrups, elixirs or suspensions may be exemplified.
  • the powdered drug can be prepared by powdering the effective component into an appropriate particle size.
  • the powders can be prepared by powdering the effective component into an appropriate particle size, and then mixing with a pharmaceutically acceptable carrier which has been powdered similarly, such as carbohydrates such as starch and mannitol and another excipients.
  • a pharmaceutically acceptable carrier which has been powdered similarly, such as carbohydrates such as starch and mannitol and another excipients.
  • the powdered drug and the powders may contain, if necessary, flavoring agents, preservatives, dispersers, colorants, aromas, etc.
  • the capsules can be prepared by filling the above powdered-drug, powders or granules into the external skin of a capsule such as gelatin capsule.
  • the powdered-drug, powders, granules may be mixed with lubricants, fluidizing agents e.g., colloidal silica, talc, magnesium stearate, calcium stearate, solid polyethylene glycol etc.
  • lubricants e.g., colloidal silica, talc, magnesium stearate, calcium stearate, solid polyethylene glycol etc.
  • disintegrants and plasticizers such as carboxymethyl cellulose, calcium carboxymethyl cellulose, hydroxypropyl cellulose having a lower degree of substitution, sodium croscarmellose, sodium carboxystarch, calcium carbonate, sodium carbonate and the like, may be added to them.
  • the granules can be prepared by mixing the powdered effective component and the above excipients and disintegrants, and adding binders (e.g., sodium carboxymethyl cellulose, hydroxypropylcellulose, methylcellulose, hydroxy propylmethylcellulose, gelatin, polyvinyl pyrrolidone, polyvinyl alcohol) and humectants (e.g., syrups, starch glue, gum arabic, cellulose solution or high-molecule material solutions) to them and kneading, and then force-passing them through sieves.
  • binders e.g., sodium carboxymethyl cellulose, hydroxypropylcellulose, methylcellulose, hydroxy propylmethylcellulose, gelatin, polyvinyl pyrrolidone, polyvinyl alcohol
  • humectants e.g., syrups, starch glue, gum arabic, cellulose solution or high-molecule material solutions
  • Solution retarder e.g., paraffin, wax, hardened castor oil
  • reabsorbent e.g., quaternary salts
  • adsorbent e.g., bentonite, kaolin, dicalcium phosphate
  • the tablets may be prepared by adding stearic acid, stearate, talc, mineral oils as tablet lubricant to the granules thus obtained, and tabletting.
  • coating of a high-molecular material such as sugar, transparent or semi-transparent protective coating comprising sealed coating of shellac, polishing coating comprising wax and the like may be provided on the obtained uncoated-tablet.
  • the effective component may be tabletted directly after mixing with fluid inactive carriers, without steps such as the granulating or the slugging.
  • the syrups may be prepared by dissolving effective component in an appropriate flavored aqueous solution.
  • the elixirs may be prepared by dissolving effective component in a non-toxic alcohol carrier.
  • the suspensions may be prepared by dissolving effective component in a non-toxic carrier.
  • suspending agents e.g., ethoxylated isostearyl alcohols, polyoxyethylene sorbitol esters
  • preservatives e.g., peppermint oil, saccharin
  • flavoring agent e.g., peppermint oil, saccharin
  • the formulation for parenteral administration includes formulations for subcutaneous, intramuscular, intraarterial and intravenous administrations.
  • the formulation for parenteral administration may be formed into solutions and suspensions.
  • the formulation for parenteral administration may be prepared by dissolving or suspending a determined amount of the effective component into a non-toxic liquid carrier suitable for the purpose of the injection such as aqueous or oily solutions, and then sterilizing the solution or suspension.
  • the formulation for parenteral administration may be prepared by filling a determined amount of the powdered or freeze-dried compound of the present invention into a vial and sterilizing the vial and its content, which is dissolved in or mixed with carrier just before an administration.
  • a non-toxic salt or a salt solution may be added, and solubilizers, preservatives, suspending agents and emulsifying agents may be used together.
  • the formulation for intrarectal administration may be prepared by kneading the effective component into a hydrophobic or hydrophilic suppository base, e.g., a synthesized oily base such as cacao oil, hydrogenated peanuts oil, hydrogenated coconuts oil, an aqueous base such as polyethylene glycol, monolene, Tween, Pluronic, higher esters (e.g., palmitic acid myristyl ester).
  • a hydrophobic or hydrophilic suppository base e.g., a synthesized oily base such as cacao oil, hydrogenated peanuts oil, hydrogenated coconuts oil, an aqueous base such as polyethylene glycol, monolene, Tween, Pluronic, higher esters (e.g., palmitic acid myristyl ester).
  • plasters, poultices, ointments, gels, creams, gel creams, liniments may be exemplified.
  • the plasters may be prepared by formulating plaster bases, the effective component and another additives, applying them onto an flexible or non-flexible backing, and applying releasable cover.
  • the flexible or non-flexible backing e.g., polypropylene, polyester, polyvinyliden chloride, polyacryl, polyurethane, rayon, cotton, ethylene-vinyl acetate copolymer, unwoven fabric and unwoven paper may be exemplified.
  • the plaster bases may be selected and used from known high-molecular bases (e.g., methacrylic esters, acrylonitrile, acrylic compositions which are copolymerized with vinyl monomer such as vinyl acetate and vinyl propionate; silicone resins; polyisoprene rubber; polyisobutylene rubber; natural rubber; acrylic rubber; styrene-isoprene-styrene block copolymer), oil or higher fatty acid (e.g., almond oil, olive oil, camellia oil, Persic oil, peanut oil, oleic acid, liquid paraffin, polybutene), tackifiers (e.g., rosin, rosin modified maleic acid, hydrogenated rosin ester), anti-eruption agent.
  • known high-molecular bases e.g., methacrylic esters, acrylonitrile, acrylic compositions which are copolymerized with vinyl monomer such as vinyl acetate and vinyl propionate
  • silicone resins poly
  • dl-camphor As another additives, dl-camphor, l-menthol, thymol, vanillyl amide nonylate, capsicum tincture, peppermint oil, UV absorber, antioxidant, may be exemplified.
  • the plasters may be a reservoir type.
  • the poultices may be prepared by formulating poultice bases, the effective component and another additives appropriately.
  • the poultice bases are selective suitably from, e.g., adhesives (e.g., synthesized water-soluble high-molecular materials such as soda polyacrylate, polyacrylic acid, POVAL, polyvinyl pyrrolidone, polyethylene oxide, polyvinyl methacrylate; natural materials such as gum arabic, starch and gelatin; methylcellulose, hydroxypropylcellulose, alginic acid, sodium alginate, ammonium alginate, sodium carboxymethylcellulose), humectants (e.g., urea, glycerine, propylene glycol, butylene glycol, sorbitol), fillers (e.g., kaoline, zinc oxide, talc, titanium, bentonite, epoxy resins), organic acids (e.g., citric acid, tartaric acid, maleic acid, succinic acid), calcium,
  • the ointments may be prepared by formulating ointment bases, the effective component and another additives appropriately.
  • ointment bases any known bases may be used.
  • the ointment bases may be selected and used from higher fatty acids or esters thereof (e.g., adipic acid, myristic acid, palmitic acid, stearic acid, oleic acid, adipic acid ester, myristic acid ester, palmitic acid ester, diethyl sebacate, hexyl laurate, cetyl isooctate), waxes (e.g., spermaceti, beeswax, ceresin), surfactants (e.g., polyoxyethylene alkylether phosphoric ester), higher alcohols (e.g., cetanol, stearyl alcohol, cetostearyl alcohol), silicone oils (e.g., dimethyl polysiloxane, methylphenyl siloxane, glycolmethyl
  • the gells may be prepared by formulating gel bases, the effective component and another additives appropriately.
  • the gel bases any known ones may be used, and lower alcohols (e.g., ethanol, isopropyl alcohol), water, gelling agents (e.g., carboxyvinyl polymer, hydroxyethyl cellulose, ethyl cellulose, carboxymethyl cellulose, alginic acid propylene glycol ester), neutralizing agents (e.g., triethanol amine, diisopropanol amine, sodium hydroxide), surfactants (e.g., sorbitan sesquioleate, sorbitan trioleate, sorbitan monooleate, sorbitan monostearate, sorbitan monolaurate, polyethylene glycol monostearate, polyoxyethylene nonylphenyl ether, polyoxyethylene lauryl ether) and anti-eruption agents may be exemplified. These materials may be selected suitably.
  • l-menthol e
  • the creams may be prepared by formulating cream bases, the effective component and another additives appropriately.
  • the cream bases any known ones may be used, and higher fatty acid esters (e.g., myristic acid esters, palmitic acid esters, diethyl sebacate, hexyl laurate, cetyl isooctate), lower alcohols (e.g., ethanol, isopropanol), hydrocarbons (e.g., liquid paraffin, squalane), polyhydroxy alcohols (e.g., propylene glycol, 1,3-butylene glycol), higher alcohols (e.g., 2-hexyl decanol, cetanol, 2-octyl dodecanol), emulsifiers (e.g., polyoxyethylene alkyl ethers, fatty acid esters, polyethylene glycol fatty acid esters), preservatives (e.g., p-oxy benzoic acid ester) and anti-eruption may be exemp
  • the gel creams which have medium characteristics of the creams and the gels may be prepared by adding gelling agent (e.g., carboxy vinyl polymers, hydroxyethyl cellulose, hydroxypropyl cellulose, ethyl cellulose, carboxymethyl cellulose) and neutralizing agent (e.g., diisopropanol amine, triethanol amine, sodium hydroxide) to the creams and adjusting pH to 4 to 8, preferably to 5 to 6.5.
  • gelling agent e.g., carboxy vinyl polymers, hydroxyethyl cellulose, hydroxypropyl cellulose, ethyl cellulose, carboxymethyl cellulose
  • neutralizing agent e.g., diisopropanol amine, triethanol amine, sodium hydroxide
  • the liniments may be prepared by formulating an effective component, UV absorbers, and if necessary, antioxidants, neutralizing agents for the adjustment of pH, tackifiers (e.g., methylcellulose, carboxyvinyl polymer, hydroxypropyl cellulose), anti-eruption agents and another additives (e.g., l-menthol, camphor, peppermint oil, thymol, crotamiton, propylene carbonate, diisopropyl adipate) into alcohols (e.g., monohydroxy alcohols such as ethanol, propanol, isopropanol, polyhydroxy alcohols such as polyethylene glycol, propylene glycol, butylene glycol), water, fatty acid esters (e.g., each ester of adipic acid, sebacic acid, myristic acid) and surfactants (e.g., polyoxyethylene alkyl ether).
  • tackifiers e.g., methylcellulose, carboxyvinyl polymer
  • the dose of the compound (I), (Ia) or (Ib) or the pharmaceutically acceptable acid addition salt thereof of the present invention is properly determined depending on the conditions, ages, sexes, body weights and the like of the subjects of the administration. However, it is preferable to administer it normally approx. 10 to 500 mg per one time about one to a several times a day when administered for an adult.
  • a method for preparing the compounds and the pharmaceutically acceptable acid addition salts thereof of the present invention will be explained with an example.
  • the method for preparing the compounds and the pharmaceutically acceptable acid addition salts of the present invention are not limited by the example. ##STR5## wherein, Y 1 represents halogen, mesyl or tosyl, Y 2 represents halogen, R, R 1 , R 2 , X and n are as defined above.
  • 3-amino-2-substituted pyridine and formyl compound (II) are reacted in an inactive solvent such as a lower alcohol (e.g., methanol, ethanol) and acetic acid, in the presence of a reducing agent such as cyano sodium borohydride, triacetoxy sodium borohydride and formic acid at 20° to -50° C. to obtain a compound (III) without isolating an imine of intermediate.
  • an inactive solvent such as a lower alcohol (e.g., methanol, ethanol) and acetic acid
  • the formyl compound (II) can be prepared by the method described in e.g., Yakugakuzasshi,81(3),453-457(1961), Chem.Pharm.Bull.,38(6)1609-1615(1990) and Chem.Pharm.Bull.,42(1)95-100(1994)).
  • the compound (IV) thus obtained is hydrogenated in an inactive solvent such as a lower alcohol (e.g., methanol, ethanol) and acetic acid, in the presence of a metal catalyst such as palladium carbon, platinum oxide and Raney-nickel under 1 to 5 atmospheric pressure to obtain a compound (V).
  • an inactive solvent such as a lower alcohol (e.g., methanol, ethanol) and acetic acid
  • a metal catalyst such as palladium carbon, platinum oxide and Raney-nickel under 1 to 5 atmospheric pressure
  • Any acid addition salts may be prepared from the free bases. Namely, by mixing the compound (V) and (R)-(-)-mandelic acid in an inactive solvent such as methanol, ethanol or isopropanol and recrystallizing the produced mandelate, a diastereomer salt of (+)isomer having a high optical purity can be prepared. Further, the salt is partitioned between an organic solvent such as ether, chloroform and dichloromethan, and an aqueous inorganic base such as sodium bicarbonate, sodium carbonate and sodium hydroxide to obtain the compound (I) which is (+)enantiomer as free base. Further, by adding e.g., ether containing hydrogen chloride to the free base, an hydrochloride can be prepared.
  • an organic solvent such as ether, chloroform and dichloromethan
  • an aqueous inorganic base such as sodium bicarbonate, sodium carbonate and sodium hydroxide
  • the obtained diastereomer salt was partitioned into 1M aqueous sodium hydroxide solution and dichloromethane, and extracted three times with 10 ml of dichloromethane under alkaline condition. After drying the organic layer, it was concentrated to solidify, an oily free base was obtained.
  • a coating solution comprising ethyl cellulose, polyvinyl pyrrolidone K30, talc and ethyl alcohol was spray-coated in the conventional method so as to obtain a sustained-release formulation.
  • the granules were filled into a capsule to prepare a capsule containing 100 mg of the compound of the present invention.
  • the above-component (1) was dissolved in the (4) and (5), previously.
  • the above-component (1) was added to (2) and (3), and mixed sufficiently to prepare an aqueous formulation for parenteral administration.
  • An ointment was prepared in the conventional method using the above-components (1) to (4).
  • suppositories were prepared in the conventional method.
  • a plaster was prepared by the conventional method.
  • the receptor-binding test (A), the bioassay test using guinea pig ileum (B), the antagonism test on Substance P-induced air way edema (C), and the anti-emetic test (D) to cisplatin-induced emesis and toxicity test (E) of the compounds of the present invention will be shown.
  • test was carried out based on the method described in Y. Shimohigashi, H. Matsumoto, Y. Takano et al., Biochem.Biophys.Res.Commun., 193(No.2),624-630(1993)).
  • the pellets were re-suspended in the buffer solution (1) and centrifuged at 48,000 ⁇ G for 15 minutes.
  • the buffer solution (2) 50 mM tris.HCl buffer solution containing 10 mM ethylenediaminetetraacetic acid and 300 mM KCl, pH 7.4 was added to the pellets and suspended to be reacted under ice-cooling for 60 minutes.
  • the resulted reaction materials were centrifuged at 48,000 ⁇ G for 15 minutes. After suspending the pellets in the buffer solution (1) and distributing, the mixture were centrifuged at 48,000 ⁇ G for 15 minutes.
  • the pellets were stored at -80° C. until used as receptor samples.
  • receptor samples were suspended in 50 mM tris-HCl buffer solution to be used.
  • buffer solution binding buffer solution (tris.HCl buffer solution containing 0.02% bovine serum albumin, 40 ⁇ g/ml bacitracin, 4 ⁇ g/ml chymostatin, 4 ⁇ g/ml leupeptin and 3 mM MnCl 2 , pH7.4) was used.
  • reaction conditions 125 I!SP50pM was used as a ligand, and the reaction temperature and time were at 22° C. and for 20 minutes. The results will be shown in Table 1.
  • test was carried out based on the method described in Hiroshi Morimoto, Masako Murai, Yasue Maeda et al., J.Pharmacol.Exp.Ther., 262(No.1),398-402(1992)).
  • Substance P containing 200 I.U./kg of heparin were administered intravenously to heartley male guinea pigs in order to induce airway edema. After ten minutes, the guinea pigs were exsanguinated deadly. The amounts of the dye transudated into trachea and main bronchi were determined. 1 mg/kg of the subject compounds were administered orally at thirty minutes before the induction. The results will be shown in Table 2 as the inhibition rates compared to the control group. Further, for comparison, the following compounds A and B were used.
  • the test was carried out using male ferret (approx. 1.5 kg.). Emesis was induced by intraperitoneal administration of cisplatin (10 mg/kg). 1 mg/kg of the subject compounds were administered orally just after the cisplatin administration. The results will be shown in Table 3 as the inhibition rates compared to the control group, using the number of vomits as indexes. Further, for comparisons, the following compounds A and C were used.
  • the piperidine derivatives of the present invention have a distinguished antagonism on Substance P.
  • the piperidine derivatives of the present invention therefore, are expected to be used as a preventive or remedy for a variety of diseases mediated by Substance P and are useful for pharmaceutical industries.

Abstract

Piperidine derivatives represented by general formula (I) ##STR1## or pharmaceutically acceptable acid addition salts thereof: wherein n represents an integer of 0 or 1; X represents CH2, O or CH--CH3 ; R represents hydrogen, halogen, lower alkyl, hydroxy, lower alkoxy, lower alkylthio, lower alkylsulfinyl, lower alkylsulfonyl, substituted aminosulfonyl or nitro; R1 and R2 may be the same or different and each represents hydrogen or lower alkyl, are disclosed. The piperidine derivatives have an antagonism on Substance P and is useful as a preventive or remedy for asthma, vomiting, etc.

Description

This application is a 371 of PCT/JP96/00796 filed Mar. 27, 1996.
TECHNICAL FIELD
The present invention relates to new piperidine derivatives having an antagonism on Substance P, being a peptide neurotransmitter, and pharmaceutically acceptable acid addition salts thereof. The piperidine derivatives and pharmaceutically acceptable acid addition salts thereof of the present invention are useful as a preventive or remedy for respiratory system diseases, central nervous system diseases, digestive system diseases, circulatory system diseases, and a variety of inflammation and pains and the like.
PRIOR ART
Substance P is a tachykinin undecapeptide which is found especially in mammals and which is referred as Neurokinin with Neurokinin A and Neurokinin B etc. The facts that Substance P is involved in a variety of pathological fields such as respiratory system diseases such as asthma, central nervous system diseases such as anxiety, schizophrenia, digestive system diseases such as ulcerative colitis, circulatory system diseases such as hypertension, various inflammation and pains, have been well-known (e.g., Journal of Medicinal Chemistry,25,1009, (1982), Trends in Cluster Headache, 85-97, (1987),ELSEVIER).
In addition, until now, as the non-peptide Substance P antagonist, a compound having a quinuclidine skeleton (JP 3-503768, A), a compound having a piperidine skeleton (JP 4-103570, A), a compound having an isoindolone skeleton (JP 3-176469, A), a compound having an arylalkylamine skeleton (JP 3-206086, A) etc. have been known.
As the compounds having benzofuran ring or benzopyran ring, the compound described in WO93/09116 has been known. The non-aromatic alicyclic compound substituted by an aminomethylene group is disclosed in WO94/13663. A remedy for vomiting is disclosed in JP 7-53362, A. The compounds of the present invention are included in the compounds described in WO94/13663 and JP 7-53362, as subordinate concepts. However, the compounds of the present invention as well as the similar compounds are not disclosed in any publications concretely.
DISCLOSURE OF THE INVENTION
The object of the present invention is to provide piperidine derivatives or pharmaceutically acceptable acid addition salts thereof having an antagonism on non-peptide Substance P.
The present invention provides piperidine derivatives represented by general formula (I) ##STR2## or pharmaceutically acceptable acid addition salts thereof: wherein n represents an integer of 0 or 1; X represents CH2, O or CH--CH3 ; R represents hydrogen, halogen, lower alkyl, hydroxy, lower alkoxy, lower alkylthio, lower alkylsulfinyl, lower alkylsulfonyl, substituted aminosulfonyl or nitro; R1 and R2 may be the same or different and each represents hydrogen or lower alkyl.
The present invention also provides cis-piperidine derivatives represented by general formula (Ia) ##STR3## or pharmaceutically acceptable acid addition salts thereof: wherein n, X, R, R1 and R2 are as defined above.
The present invention also provides cis-piperidine derivatives represented by general formula (Ib) ##STR4## or pharmaceutically acceptable acid addition salts thereof: wherein R, R1 and R2 are as defined above.
The present invention also provides the piperidine derivatives or pharmaceutically acceptable acid addition salts thereof having an antagonism on Substance P.
The present invention also provides a pharmaceutical composition comprising an effective amount of the piperidine derivative or pharmaceutically acceptable acid addition salt thereof, and a pharmaceutically acceptable carrier.
The present invention also provides a preventive or remedy for asthma which comprises the piperidine derivative or pharmaceutically acceptable acid addition salt thereof as an effective component.
The present invention also provides a preventive or remedy for vomiting which comprises the piperidine derivative or pharmaceutically acceptable acid addition salt thereof as an effective component.
The present invention also provides a formulation for oral administration, a formulation for parenteral administration, a formulation for intrarectal administration or a formulation for percutaneous administration which comprises the piperidine derivative or pharmaceutically acceptable acid addition salt thereof as an effective component.
The present invention will be explained, hereinafter.
The compounds represented by the general formula (I), (Ia) and (Ib) of the present invention will be explained concretely.
In the above general formulas (I), (Ia) and (Ib), n represents an integer of 0 or 1. When n is 0, a form of condensed five-membered ring with benzen ring is shown. When n is 1, a form of condensed six-membered ring with benzen ring is shown.
X represents CH2, O or CH--CH3 substituted by a methyl group from methylene group in the ring.
In the formulas, R represents a substituent group on the phenyl group in the condensed ring, including non-substituted condition. R represents hydrogen, halogen, lower alkyl, hydroxy, lower alkoxy, lower alkylthio, lower alkylsulfinyl, lower alkylsulfonyl, substituted aminosulfonyl or nitro.
In the specification, halogen means fluorine, chlorine, bromine or iodine.
The lower alkyl group represents a cyclic or acyclic alkyl group having C1-6 which may contain one to five halogen such as fluorine in any position. As the lower alkyl group, methyl, ethyl, n-propyl, iso-propyl, n-butyl, iso-butyl, tert-butyl, n-pentyl, n-hexyl, cyclopentyl, cyclohexyl, monofluoromethyl, difluoromethyl, trifluoromethyl, trifluoro-ethyl and perfluoroethyl may be exemplified.
The lower alkoxy group represents a cyclic or acyclic alkoxy group having C1-6 which may contain one to five halogen such as fluorine in any position. As the lower alkoxy group, methoxy, ethoxy, n-propoxy, iso-propoxy, n-butoxy, iso-butoxy, tert-butoxy, n-pentyloxy, n-hexyloxy, cyclopentyloxy, cyclohexyloxy, monofluoromethoxy, difluoromethoxy, trifluoromethoxy, trifluoroethoxy and perfluoroetyoxy may be exemplified.
The lower alkylthio group represents a cyclic or acyclic alkylthio group having C1-6 which may contain one to five halogen atoms such as fluorine in any position. As the lower alkylthio group, methylthio, ethylthio, n-propylthio, iso-propylthio, n-butylthio, iso-butylthio, tert-butylthio, n-pentylthio, n-hexylthio, cyclopentylthio, cyclohexylthio, monofluoromethylthio, difluoromethylthio, trifluoromethylthio, trifluoroethylthio, perfluoroethylthio may be exemplified.
As the lower alkylsulfinyl group represents a cyclic or acyclic alkylsulfinyl group having C1-6 which may contain one to five halogen atoms such as fluorine in any position. As the lower alkylsulfinyl group, methylsulfinyl, ethylsulfinyl, n-propylsulfinyl, iso-propylsulfinyl, n-butylsulfinyl, iso-butylsulfinyl, tert-butylsulfinyl, n-pentylsulfinyl, n-hexylsulfinyl, cyclopentylsulfinyl, cyclohexylsulfonyl, monofluoromethylsulfinyl, difluoromethylsulfinyl, trifluoromethylsulfinyl, trifluoroethylsulfinyl, perfluoroethylsulfinyl may be exemplified.
The lower alkylsulfonyl group represents a cyclic or acyclic alkylsulfonyl group having C1-6 which may contain one to five halogen atoms such as fluorine in any position. As the lower alkylsulfonyl group, methylsulfonyl, ethylsulfonyl, n-propylsulfonyl, iso-propylsulfonyl, n-butylsulfonyl, iso-butylsulfonyl, tert-butylsulfonyl, n-pentylsulfonyl, n-hexylsulfonyl, cyclopentylsulfonyl, cyclohexylsulfonyl, monofluoromethylsulfonyl, difluoromethylsulfonyl, trifluoro-methylsulfonyl, trifluoroethylsulfonyl, perfluoroethyl-sulfornyl may be exemplified.
The substituted aminosulfonyl group represents a cyclic or acyclic alkylaminosulfonyl group having C1-6 which may contain one to five halogen atoms such as fluorine in any position, and represents an aminosulfonyl group in which an amino group forms a part of the cyclic compound. As the substituted aminosulfonyl group, methylaminosulfonyl, ethylaminosulfonyl, n-propylaminosulfonyl, iso-propylaminosulfonyl, n-butylaminosulfonyl, iso-butylaminosulfonyl, tert-butylaminosulfonyl, n-pentylaminosulfonyl, n-hexylaminosulfonyl, dimethylaminosulfonyl, diethylaminosulfonyl, di-n-propylaminosulfonyl, diisopropylaminosulfonyl, di-n-butylaminosulfonyl, diisobutylaminosulfonyl, cyclopentylaminosulfonyl, cyclohexylaminosulfonyl, monofluoromethylaminosulfonyl, difluoromethylaminosulfonyl, trifluoromethylaminosulfonyl, trifluoroethylaminosulfonyl, perfluoroethylaminosulfonyl, 1-pyrrolidinylsulfonyl, 1-piperidinylsulfonyl, 1-dihydropyrrolidinylsulfonyl, 1-dihydropyridinylsulfonyl may be exemplified.
R1 and R2 may be the same or different and each represents hydrogen or a lower alkyl. As the lower alkyl group, methyl, ethyl, n-propyl, isopropyl, n-butyl, isobutyl may be exemplified. Depending on the combination of R1 and R2, the forms of unsubstitution, monoalkyl and dialkyl may be made.
The present invention includes any forms of stereoisomers produced in monoalkyl, diastereomer and mixtures thereof. In addition, the present invention includes both of cis-isomer and trans-isomer of the compound (I), among which cis-isomer represented by the formula (Ia) is most preferable.
As examples of the pharmaceutically acceptable acid addition salts, salts formed with an inorganic acid such as hydrochloric acid, hydrobromic acid, sulfuric acid, nitric acid, phosphoric acid: or salts formed with an organic acid such as acetic acid, propionic acid, glycolic acid, lactic acid, malic acid, tartaric acid, citric acid, ascorbic acid, maleic acid, oxalic acid, fumaric acid, succinic acid, malonic acid, methanesulfonic acid, benzensulfonic acid, toluene-sulfonic acid, may be exemplified. The acid addition salts are, however, not limited by the examples.
As preferable examples of the compounds represented by the general formula (I) and the acid addition salts thereof,
(2S,3S)-3- (2,2-dimethyl-2,3-dihydrobenzofuran-7-yl)methyl!amino-2-phenylpiperidine hydrochloride,
(2S,3S)-3- (2-methyl-2,3-dihydrobenzofuran-7-yl)methyl!amino-2-phenylpiperidine hydrochloride,
(2S,3S)-3- (2,2-dimethyl-5-nitro-2,3-dihydrobenzofuran-7-yl)methyl!amino-2-phenylpiperidine hydrochloride,
(2S,3S)-3- (2,2-dimethyl-5-methylthio-2,3-dihydrobenzofuran-7-yl)methyl!amino-2-phenylpiperidine hydrochloride,
(2S,3S)-3- (2,2-dimethyl-5-methylsulfonyl-2,3-dihydrobenzofuran-7-yl)methyl!amino-2-phenylpiperidine hydrochloride,
(2S,3S)-3- (2,2-dimethyl-5-dimethylaminosulfonyl-2,3-dihydrobenzofuran-7-yl)methyl!amino-2-phenylpiperidine hydrochloride,
(2S,3S)-3- (5-dimethylaminosulfonyl-2-methyl-2,3-dihydrobenzofuran-7-yl)methyl!amino-2-phenylpiperidine hydrochloride,
(2S,3S)-3-(3,4-methylenedioxybenzyl)amino-2-phenyl-piperidine hydrochloride,
(2S,3S)-3- (3,4-dihydro-1,2-benzopyran-8-yl)methyl!amino-2-phenylpiperidine hydrochloride,
(2S,3S)-3- (5-chloro-2,2-dimethyl-2,3-dihydrobenzofuran-7-yl)methyl!amino-2-phenylpiperidine hydrochloride,
(2S,3S)-3- (2,2-dimethyl-5-methoxy-2,3-dihydrobenzofuran-7-yl)methyl!amino-2-phenylpiperidine hydrochloride,
(2S,3S)-3- (2,3-dihydrobenzofuran-7-yl)methyl!amino-2-phenylpiperidine hydrochloride,
(2S,3S)-3- (5-chloro-2-methyl-2,3-dihydrobenzofuran-7-yl)methyl!amino-2-phenylpiperidine hydrochloride,
(2S,3S)-3- (5-methoxy-2-methyl-2,3-dihydrobenzofuran-7-yl)methyl!amino-2-phenylpiperidine hydrochloride,
(2S,3S)-3- (2,2,4-trimethyl-2,3-dihydrobenzofuran-7-yl)methyl!amino-2-phenylpiperidine hydrochloride,
(2S,3S)-3- (2,2,5-trimethyl-2,3-dihydrobenzofuran-7-yl)methyl!amino-2-phenylpiperidine hydrochloride,
(2S,3S)-3- (4-chloro-2,2-dimethyl-2,3-dihydrobenzofuran-7-yl)methyl!amino-2-phenylpiperidine hydrochloride,
(2S,3S)-3-(3,4-methylenedioxybenzyl)amino-2-phenylpiperidine hydrochloride,
(2S,3S)-3- (2,3-dimethyl-2,3-dihydrobenzofuran-7-yl)methyl!amino-2-phenylpiperidine hydrochloride,
(2S,3S)-3- (2,3,4-trimethyl-2,3-dihydrobenzofuran-7-yl)methyl!amino-2-phenylpiperidine hydrochloride,
(2S,3S)-3- (2,5-dimethyl-2,3-dihydrobenzofuran-7-yl)methyl!amino-2-phenylpiperidine hydrochloride,
(2S,3S)-3- (5-isopropyl-2,3-dihydrobenzofuran-7-yl)methyl!amino-2-phenylpiperidine hydrochloride,
(2S,3S)-3- (5-tert.butyl-2,3-dihydrobenzofuran-7-yl)methyl!amino-2-phenylpiperidine hydrochloride,
(2S,3S)-3- (5-cyclopentyl-2,3-dihydrobenzofuran-7-yl)methyl!amino-2-phenylpiperidine hydrochloride,
(2S,3S)-3- (5-cyclohexyl-2,3-dihydrobenzofuran-7-yl)methyl!amino-2-phenylpiperidine hydrochloride,
(2S,3S)-3- (5-ethylthio-2,3-dihydrobenzofuran-7-yl)methyl!amino-2-phenylpiperidine hydrochloride,
(2S,3S)-3- (5-isopropylthio-2,3-dihydrobenzofuran-7-yl)methyl!amino-2-phenylpiperidine hydrochloride,
(2S,3S)-3- (5-cyclohexylthio-2,3-dihydrobenzofuran-7-yl)methyl!amino-2-phenylpiperidine hydrochloride,
(2S,3S)-3- (5-trifluoromethylthio-2,3-dihydro-benzofuran-7-yl)methyl!amino-2-phenylpiperidine hydrochloride,
(2S,3S)-3- (5-(2,2,2-trifluoro)ethylthio-2,3-dihydrobenzofuran-7-yl)methyl!amino-2-phenylpiperidine hydrochloride,
(2S,3S)-3- (5-methylsulfinyl-2,3-dihydrobenzofuran-7-yl)methyl!amino-2-phenylpiperidine hydrochloride,
(2S,3S)-3- (5-isopropylsulfonyl-2,3-dihydrobenzofuran-7-yl)methyl!amino-2-phenylpiperidine hydrochloride,
(2S,3S)-3- (5-isopropylsulfonyl-2-methyl-2,3-dihydrobenzofuran-7-yl)methyl!amino-2-phenylpiperidine hydrochloride,
(2S,3S)-3- (5-cyclopentylsulfonyl-2,3-dihydrobenzofuran-7-yl)methyl!amino-2-phenylpiperidine hydrochloride,
(2S,3S)-3- (2-methyl-5-methylaminosulfonyl-2,3-dihydrobenzofuran-7-yl)methyl!amino-2-phenylpiperidine hydrochloride,
(2S,3S)-3- (5-methoxy-2,3-dihydrobenzofuran-7-yl)methyl!amino-2-phenylpiperidine hydrochloride,
(2S,3S)-3- (2,2-dimethyl-5-fluoro-2,3-dihydrobenzofuran-7-yl)methyl!amino-2-phenylpiperidine hydrochloride,
(2S,3S)-3- (5-hydroxy-2-methyl-2,3-dihydrobenzofuran-7-yl)methyl!amino-2-phenylpiperidine hydrochloride,
(2S,3S)-3- (5-fluoro-2-methyl-2,3-dihydrobenzofuran-7-yl)methyl!amino-2-phenylpiperidine hydrochloride,
(2S,3S)-3- (5-nitro-2,3-dihydrobenzofuran-7-yl)methyl!amino-2-phenylpiperidine hydrochloride,
(2S,3S)-3- (2-methyl-5-methylsulfonyl-2,3-dihydrobenzofuran-7-yl)methyl!amino-2-phenylpiperidine hydrochloride,
(2S,3S)-3- (2-methyl-5-methylthio-2,3-dihydrobenzofuran-7-yl)methyl!amino-2-phenylpiperidine hydrochloride,
(2S,3S)-3- (5-dimethylaminosulfonyl-2,3-dihydrobenzofuran-7-yl)methyl!amino-2-phenylpiperidine hydrochloride,
(2S,3S)-3- (5-methylsulfonyl-2,3-dihydrobenzofuran-7-yl)methyl!amino-2-phenylpiperidine hydrochloride,
(2S,3S)-3- (5-methylthio-2,3-dihydrobenzofuran-7-yl)methyl!amino-2-phenylpiperidine hydrochloride,
(2S,3S)-3- (5-methyl-2,3-dihydrobenzofuran-7-yl)methyl!amino-2-phenylpiperidine hydrochloride,
(2S,3S)-3- (5-chloro-2,3-dihydrobenzofuran-7-yl)methyl!amino-2-phenylpiperidine hydrochloride,
(2S,3S)-3- (5-ethoxy-2-methyl-2,3-dihydrobenzofuran-7-yl)methyl!amino-2-phenylpiperidine hydrochloride,
(2S,3S)-3- (5-cyclopentyloxy-2-methyl-2,3-dihydro-benzofuran-7-yl)methyl!amino-2-phenylpiperidine hydrochloride,
(2S,3S)-3- (2,4-dimethyl-5-dimethylaminosulfonyl-2,3-dihydrobenzofuran-7-yl)methyl!amino-2-phenylpiperidine hydrochloride,
(2S,3S)-3- (2-methyl-5-(1-pyrrolidinyl)sulfonyl-amino-2,3-dihydrobenzofuran-7-yl)methyl!amino-2-phenylpiperidine hydrochloride, and
(2S,3S)-3- (5-trifluoromethoxy-2,3-dihydrobenzofuran-7-yl)methyl!amino-2-phenylpiperidine hydrochloride, may be exemplified.
The piperidine derivatives and pharmaceutically acceptable acid addition salts thereof of the present invention are useful as a preventive or remedy for respiratory system diseases, central nervous system diseases, digestive system diseases, circulatory system diseases, and a variety of inflammation and pains and the like. As concrete examples of these diseases and inflammations, chronic bronchial obstruction, asthma, migraine, vomiting, anxiety, depression, melancholia, Alzheimer's diseases, dementia, stomatosis caused by stress, anaphylaxis, colitis, hypertension, vasospamic diseases, hidebound disease, arthritis, psoriasis, rheumatic diseases, multiple sclerosis, systemic lupus erythematosus, initis, drug toxicosis may be exemplified.
When the compound represented by the general formula (I), (Ia) or (Ib) or the pharmaceutically acceptable acid addition salt thereof is administered as a drug, it may be administered as it is, or it may be made into any forms of formulations for oral administration, parenteral administration, intrarectal administration and percutaneous administration together with known carriers.
The formulation for oral administration is not limited to, but solid or liquid formulations such as powdered drug, powders, capsules, granules, tablets, syrups, elixirs or suspensions may be exemplified.
The powdered drug can be prepared by powdering the effective component into an appropriate particle size. The powders can be prepared by powdering the effective component into an appropriate particle size, and then mixing with a pharmaceutically acceptable carrier which has been powdered similarly, such as carbohydrates such as starch and mannitol and another excipients. The powdered drug and the powders may contain, if necessary, flavoring agents, preservatives, dispersers, colorants, aromas, etc.
The capsules can be prepared by filling the above powdered-drug, powders or granules into the external skin of a capsule such as gelatin capsule. Before filling, the powdered-drug, powders, granules may be mixed with lubricants, fluidizing agents e.g., colloidal silica, talc, magnesium stearate, calcium stearate, solid polyethylene glycol etc. In addition, disintegrants and plasticizers such as carboxymethyl cellulose, calcium carboxymethyl cellulose, hydroxypropyl cellulose having a lower degree of substitution, sodium croscarmellose, sodium carboxystarch, calcium carbonate, sodium carbonate and the like, may be added to them.
The granules can be prepared by mixing the powdered effective component and the above excipients and disintegrants, and adding binders (e.g., sodium carboxymethyl cellulose, hydroxypropylcellulose, methylcellulose, hydroxy propylmethylcellulose, gelatin, polyvinyl pyrrolidone, polyvinyl alcohol) and humectants (e.g., syrups, starch glue, gum arabic, cellulose solution or high-molecule material solutions) to them and kneading, and then force-passing them through sieves. Alternatively, instead of granulating powders in such a way, after treating powders with a tablet press, the obtained incomplete forms of slugs may be powdered to obtain granules. Solution retarder (e.g., paraffin, wax, hardened castor oil), reabsorbent (e.g., quaternary salts) or adsorbent (e.g., bentonite, kaolin, dicalcium phosphate) may be mixed in previously.
The tablets may be prepared by adding stearic acid, stearate, talc, mineral oils as tablet lubricant to the granules thus obtained, and tabletting. In addition, coating of a high-molecular material such as sugar, transparent or semi-transparent protective coating comprising sealed coating of shellac, polishing coating comprising wax and the like may be provided on the obtained uncoated-tablet. The effective component may be tabletted directly after mixing with fluid inactive carriers, without steps such as the granulating or the slugging.
The syrups may be prepared by dissolving effective component in an appropriate flavored aqueous solution. The elixirs may be prepared by dissolving effective component in a non-toxic alcohol carrier. The suspensions may be prepared by dissolving effective component in a non-toxic carrier. To the syrups, elixirs and suspensions, suspending agents, emulsifying agents (e.g., ethoxylated isostearyl alcohols, polyoxyethylene sorbitol esters), preservatives, flavoring agent (e.g., peppermint oil, saccharin) and the like may be added if desired.
The formulation for parenteral administration includes formulations for subcutaneous, intramuscular, intraarterial and intravenous administrations. The formulation for parenteral administration may be formed into solutions and suspensions. The formulation for parenteral administration may be prepared by dissolving or suspending a determined amount of the effective component into a non-toxic liquid carrier suitable for the purpose of the injection such as aqueous or oily solutions, and then sterilizing the solution or suspension. Alternatively, the formulation for parenteral administration may be prepared by filling a determined amount of the powdered or freeze-dried compound of the present invention into a vial and sterilizing the vial and its content, which is dissolved in or mixed with carrier just before an administration. In order to make the formulation for parenteral administration isotonic, a non-toxic salt or a salt solution may be added, and solubilizers, preservatives, suspending agents and emulsifying agents may be used together.
The formulation for intrarectal administration may be prepared by kneading the effective component into a hydrophobic or hydrophilic suppository base, e.g., a synthesized oily base such as cacao oil, hydrogenated peanuts oil, hydrogenated coconuts oil, an aqueous base such as polyethylene glycol, monolene, Tween, Pluronic, higher esters (e.g., palmitic acid myristyl ester).
As the formulation for percutaneous administration, plasters, poultices, ointments, gels, creams, gel creams, liniments may be exemplified.
The plasters may be prepared by formulating plaster bases, the effective component and another additives, applying them onto an flexible or non-flexible backing, and applying releasable cover. As the flexible or non-flexible backing, e.g., polypropylene, polyester, polyvinyliden chloride, polyacryl, polyurethane, rayon, cotton, ethylene-vinyl acetate copolymer, unwoven fabric and unwoven paper may be exemplified. The plaster bases may be selected and used from known high-molecular bases (e.g., methacrylic esters, acrylonitrile, acrylic compositions which are copolymerized with vinyl monomer such as vinyl acetate and vinyl propionate; silicone resins; polyisoprene rubber; polyisobutylene rubber; natural rubber; acrylic rubber; styrene-isoprene-styrene block copolymer), oil or higher fatty acid (e.g., almond oil, olive oil, camellia oil, Persic oil, peanut oil, oleic acid, liquid paraffin, polybutene), tackifiers (e.g., rosin, rosin modified maleic acid, hydrogenated rosin ester), anti-eruption agent. As another additives, dl-camphor, l-menthol, thymol, vanillyl amide nonylate, capsicum tincture, peppermint oil, UV absorber, antioxidant, may be exemplified. The plasters may be a reservoir type.
The poultices may be prepared by formulating poultice bases, the effective component and another additives appropriately. The poultice bases are selective suitably from, e.g., adhesives (e.g., synthesized water-soluble high-molecular materials such as soda polyacrylate, polyacrylic acid, POVAL, polyvinyl pyrrolidone, polyethylene oxide, polyvinyl methacrylate; natural materials such as gum arabic, starch and gelatin; methylcellulose, hydroxypropylcellulose, alginic acid, sodium alginate, ammonium alginate, sodium carboxymethylcellulose), humectants (e.g., urea, glycerine, propylene glycol, butylene glycol, sorbitol), fillers (e.g., kaoline, zinc oxide, talc, titanium, bentonite, epoxy resins), organic acids (e.g., citric acid, tartaric acid, maleic acid, succinic acid), calcium, magnesium, aluminum and water. In addition, as another additives, e.g., l-menthol, camphor, thymol, peppermint oil, UW absorber and antioxidant are exemplified, and these may be formulated suitably.
The ointments may be prepared by formulating ointment bases, the effective component and another additives appropriately. As the ointment bases, any known bases may be used. The ointment bases may be selected and used from higher fatty acids or esters thereof (e.g., adipic acid, myristic acid, palmitic acid, stearic acid, oleic acid, adipic acid ester, myristic acid ester, palmitic acid ester, diethyl sebacate, hexyl laurate, cetyl isooctate), waxes (e.g., spermaceti, beeswax, ceresin), surfactants (e.g., polyoxyethylene alkylether phosphoric ester), higher alcohols (e.g., cetanol, stearyl alcohol, cetostearyl alcohol), silicone oils (e.g., dimethyl polysiloxane, methylphenyl siloxane, glycolmethyl polysiloxane, silicone glycol copolymer), hydrocarbons (e.g., hydrophilic vaseline, white vaseline, purified lanoline, liquid paraffin), water, humectants (glycerine, propylene glycol, butylene glycol, sorbitol), anti-eruption agent and the like. As another additives, l-menthol, camphor, peppermint oil and the like may be exemplified.
The gells may be prepared by formulating gel bases, the effective component and another additives appropriately. As the gel bases, any known ones may be used, and lower alcohols (e.g., ethanol, isopropyl alcohol), water, gelling agents (e.g., carboxyvinyl polymer, hydroxyethyl cellulose, ethyl cellulose, carboxymethyl cellulose, alginic acid propylene glycol ester), neutralizing agents (e.g., triethanol amine, diisopropanol amine, sodium hydroxide), surfactants (e.g., sorbitan sesquioleate, sorbitan trioleate, sorbitan monooleate, sorbitan monostearate, sorbitan monolaurate, polyethylene glycol monostearate, polyoxyethylene nonylphenyl ether, polyoxyethylene lauryl ether) and anti-eruption agents may be exemplified. These materials may be selected suitably. As another additives, l-menthol, camphor, peppermint oil and the like may be exemplified.
The creams may be prepared by formulating cream bases, the effective component and another additives appropriately. As the cream bases, any known ones may be used, and higher fatty acid esters (e.g., myristic acid esters, palmitic acid esters, diethyl sebacate, hexyl laurate, cetyl isooctate), lower alcohols (e.g., ethanol, isopropanol), hydrocarbons (e.g., liquid paraffin, squalane), polyhydroxy alcohols (e.g., propylene glycol, 1,3-butylene glycol), higher alcohols (e.g., 2-hexyl decanol, cetanol, 2-octyl dodecanol), emulsifiers (e.g., polyoxyethylene alkyl ethers, fatty acid esters, polyethylene glycol fatty acid esters), preservatives (e.g., p-oxy benzoic acid ester) and anti-eruption may be exemplified. These materials may be selected suitably. As another additives, l-menthol, camphor, peppermint oil and the like may be exemplified.
The gel creams which have medium characteristics of the creams and the gels, may be prepared by adding gelling agent (e.g., carboxy vinyl polymers, hydroxyethyl cellulose, hydroxypropyl cellulose, ethyl cellulose, carboxymethyl cellulose) and neutralizing agent (e.g., diisopropanol amine, triethanol amine, sodium hydroxide) to the creams and adjusting pH to 4 to 8, preferably to 5 to 6.5.
The liniments may be prepared by formulating an effective component, UV absorbers, and if necessary, antioxidants, neutralizing agents for the adjustment of pH, tackifiers (e.g., methylcellulose, carboxyvinyl polymer, hydroxypropyl cellulose), anti-eruption agents and another additives (e.g., l-menthol, camphor, peppermint oil, thymol, crotamiton, propylene carbonate, diisopropyl adipate) into alcohols (e.g., monohydroxy alcohols such as ethanol, propanol, isopropanol, polyhydroxy alcohols such as polyethylene glycol, propylene glycol, butylene glycol), water, fatty acid esters (e.g., each ester of adipic acid, sebacic acid, myristic acid) and surfactants (e.g., polyoxyethylene alkyl ether).
The dose of the compound (I), (Ia) or (Ib) or the pharmaceutically acceptable acid addition salt thereof of the present invention is properly determined depending on the conditions, ages, sexes, body weights and the like of the subjects of the administration. However, it is preferable to administer it normally approx. 10 to 500 mg per one time about one to a several times a day when administered for an adult.
Next, a method for preparing the compounds and the pharmaceutically acceptable acid addition salts thereof of the present invention will be explained with an example. The method for preparing the compounds and the pharmaceutically acceptable acid addition salts of the present invention are not limited by the example. ##STR5## wherein, Y1 represents halogen, mesyl or tosyl, Y2 represents halogen, R, R1, R2, X and n are as defined above.
As shown in above, at the beginning, 3-amino-2-substituted pyridine and formyl compound (II) are reacted in an inactive solvent such as a lower alcohol (e.g., methanol, ethanol) and acetic acid, in the presence of a reducing agent such as cyano sodium borohydride, triacetoxy sodium borohydride and formic acid at 20° to -50° C. to obtain a compound (III) without isolating an imine of intermediate. (The formyl compound (II) can be prepared by the method described in e.g., Yakugakuzasshi,81(3),453-457(1961), Chem.Pharm.Bull.,38(6)1609-1615(1990) and Chem.Pharm.Bull.,42(1)95-100(1994)).
Then, a cross-coupling reaction of the compound (III) thus obtained and Grignard reagent are carried out in an inactive solvent such as tetrahydrofuran (abbreviated as THF, hereinafter) and ether in the presence of a transition-metal catalyst such as {1,2-bis(diphenylphosphino) propane}nickel(II) chloride (abbreviated as NiCl2 (dppp), hereinafter) and {1,2-bis(diphenylphosphino)ethane}nickel(II) chloride (abbreviated as NiCl2 (dppe), hereinafter) at 0° to 70° C. to obtain the compound (IV).
Then, the compound (IV) thus obtained is hydrogenated in an inactive solvent such as a lower alcohol (e.g., methanol, ethanol) and acetic acid, in the presence of a metal catalyst such as palladium carbon, platinum oxide and Raney-nickel under 1 to 5 atmospheric pressure to obtain a compound (V).
Finally, the racemic mixture (V) is resolved optically to obtain the compound represented by the general formula (I) of the present invention.
Any acid addition salts may be prepared from the free bases. Namely, by mixing the compound (V) and (R)-(-)-mandelic acid in an inactive solvent such as methanol, ethanol or isopropanol and recrystallizing the produced mandelate, a diastereomer salt of (+)isomer having a high optical purity can be prepared. Further, the salt is partitioned between an organic solvent such as ether, chloroform and dichloromethan, and an aqueous inorganic base such as sodium bicarbonate, sodium carbonate and sodium hydroxide to obtain the compound (I) which is (+)enantiomer as free base. Further, by adding e.g., ether containing hydrogen chloride to the free base, an hydrochloride can be prepared.
EXAMPLES
Examples and Test Examples will be described in order to explain the present invention in more detail, hereinafter. The present invention, however, should not be limited by the Examples.
Reference Example 1
5 g of 3-amino-2-chloropyridine was dissolved in 80 ml of acetic acid, and 7.1 g of 2,2-dimethyl-7-formyl-2,3-dihydrobenzofuran was added. Then, the mixture was stirred at room temperature for about 30 minutes, and 16.5 g of triacetoxy sodium borohydride was added gradually under ice-cooling. After stirring the obtained reaction mixture at room temperature for about four hours, the solvent was concentrated. After adding ice-water to the residue and alkalizing it with an aqueous sodium hydroxide solution, it was extracted twice with ethyl acetate. After washing the organic layer with water and drying, it was concentrated and purified with a short column (dichloromethane/methanol=10:1) using silica gel to obtain 12.2 g of oily 3- (2,2-dimethyl-2,3-dihydrobenzofuran-7-yl)methyl!amino-2-chloropyridine.
MS 119,161(base),288(M+); NMR(CDCl3) 1.48(6H,s),3.00(2H,s),4.32(2H,bs),5.06(1H,br); 6.78(1H,t,J=7.5 Hz), 6.93-7.07(4H,m), 7.68(1H,dd, J=4.6 Hz,J=1.7 Hz)
Reference Example 2
12 g of 3- (2,2-dimethyl-2,3-dihydrozenbofuran-7-yl)methyl!amino-2-chloropyridine was dissolved in approx. 400 ml of anhydrous THF, and 7.8 g of NiCl2 (dppe) was added. 30 ml of 3M ether solution of phenylmagnesium bromide was added dropwise to the mixture with stirring at room temperature under nitrogen flow, and a reaction was carried out for seven hours. Further, 20 ml of 3M ether solution of phenylmagnesium bromide was added and kept stirring for 15 hours. After completion of the reaction, the reaction mixture was poured into a mixed liquid of 600 ml of conc.HCl and approx. 400 ml of ice-water, and washed with approx. 500 ml of ethyl acetate. After alkalizing the acid water layer with 50% aqueous sodium hydroxide solution with cooling, approx. 1000 ml of ethyl acetate was added and Celite was added with stirring. After the precipitates were filtered off, it was washed with 500 ml of ethyl acetate twice. The organic layer was separated, and the aqueous layer was extracted with ethyl acetate. These were combined and dried with magnesium sulfate. The residue which was obtained by distilling off the solvent, was purified by a silica gel column chromatography (isopropyl ether/hexane=1:1-isopropyl ether-isopropyl ether/ethyl acetate=1:1) to obtain 9.4 g of oily 3- (2,2-dimethyl-2,3-dihydrobenzofuran-7-yl)methyl!amino-2-phenylpyridine.
MS 119,161(base),330(M+); NMR(CDCl3) 1.38(6H,s),2.96(2H,s),4.23(2H,d,J=5.9 Hz),4.76(1H,br), 6.75(1H,t,J=7.5 Hz),7.01-7.09(4H,m),7.32-7.47 (3H,m),7.63-7.67(2H,m),8.02(1H,dd,J=4.4 Hz, J=1.8 Hz)
Reference Example 3
From 24 g of 7-ethoxycarbonyl-2-methyl-2,3-dihydrobenzofuran, 11.8 g of the former component (99.5% e.e.) and 11.6 g of the latter component (99.7% e.e.) of the optical isomers derived from methyl group in the 2-position under the following conditions.
Column: Chiral Cell OJ (Daicell)
Mobil phase: Hexane/2-propanol/acetic acid=90:10:0.3
After adding dropwise 11 g of each ester in 100 ml of anhydrous THF containing 2.2 g of lithium aluminum hydride at 0° C. under nitrogen flow, the mixture was stirred at room temperature for one hour. After completion of the reaction, ice pieces were added carefully to decompose the excessive reducing agent. Then, excessive magnesium sulphate was added and the solid materials were filtered off. The residue which was obtained by concentrating the solvent under reduced pressure, was purified by a silica gel column (isopropyl ether/hexane=1:2) to obtain 8.4 g (derived from the former component) and 8.5 g (derived from the latter component) of each corresponding 7-hydroxymethyl-2-methyl-2,3-dihydrobenzofuran were prepared.
Into a solution obtained by dissolving 8.3 g of oxalyl chloride in 30 ml of methylene chloride, a solution obtained by dissolving 8.7 g of dimethyl sulfoxide in 5 ml of methylene chloride was added dropwise at -78° C. under nitrogen flow. Further, after stirring at the same temperature for one hour, 25 g of triethyl amine was added and left to warm up to room temperature. Cold water was added to the reaction solution, and the organic phase was separated. After washing with water and drying, the solvent was concentrated under reduced pressure. The residue was purified with a silica gel column (hexane-hexane/isopropyl ether=2:1) to obtain 7.9 g (the former component) and 7.8 g (the latter component) of each corresponding 7-formyl-2-methyl-2,3-dihydrobenzofuran.
______________________________________
Enantiomer A (the former component)
                     m.p. 47-48.5° C.
                     NMR(CDCl.sub.3)1.53(3H,d,
                     J=6.23 Hz)
Enantiomer B (the latter component)
                     m.p. 47.5-49° C.
                     NMR(CDCl.sub.3)1.53(3H,d,
                     J=6.23 Hz)
______________________________________
The enantiomers of the following Reference Examples 4 to 6, based on Reference Example 3.
Reference Example 4
5-chloro-2-methyl-7-formyl-2,3-dihydrobenzofuran
______________________________________
Enantiomer A (the former component)
                     m.p. 54-55° C.
                     NMR(CDCl.sub.3)1.53(3H,d,
                     J=6.22 Hz)
Enantiomer B (the latter component)
                     m.p. 54.5-56° C.
                     NMR(CDCl.sub.3)1.53(3H,d,
                     J=6.23 Hz)
______________________________________
Reference Example 5
5-methoxy-2-methyl-7-formyl-2,3-dihydrobenzofuran
______________________________________
Enantiomer A (the former component)
                     m.p. 86-87.5° C.
                     NMR(CDCl.sub.3)1.51(3H,d,
                     J=6.22 Hz)
Enantiomer B (the latter component)
                     m.p. 57-88.5° C.
                     NMR(CDCl.sub.3)1.52(3H,d,
                     J=6.22 Hz)
______________________________________
Reference Example 6
2,5-dimethyl-7-formyl-2,3-dihydrobenzofuran
______________________________________
Enantiomer A (the former component)
                     oily material
                     NMR(CDCl.sub.3)1.52(3H,d,
                     J=6.23 Hz)
Enantiomer B (the latter component)
                     oily material
                     NMR(CDCl.sub.3)1.53(3H,d,
                     J=6.23 Hz)
______________________________________
Example 1
9.2 g of 3- (2,2-dimethyl-2,3-dihydrobenzofuran-7-yl)methyl!amino-2-phenylpyridine was dissolved in 120 ml of acetic acid, and 1 g of platinum oxide was added. A hydrogenation reaction was carried out at 3 atmospheric pressure for 8.5 hours. After completion of the reaction, the catalyst was filtered off and the solvent was concentrated. After adding ice pieces to the residue and alkalizing it with 50% aqueous sodium hydroxide solution, it was extracted three times with dichloromethane. After drying the extract solution, it was distilled off and purified by a silica gel chromatography (dichloromethane/methanol 30:1-10:1-3:1) to obtain 3.7 g of oily 3- (2,2-dimethyl-2,3-dihydrobenzofuran-7-yl)methyl!amino-2-phenylpiperidine.
MS 161(base),176,217,336(M+)
Example 2
3.63 g of 3- 2,2-dimethyl-2,3-dihydrobenzofuran-7-yl)methyl!amino-2-pheynylpiperidine which was prepared in Example 1, was dissolved in 15 ml of methanol. About 15 ml of a methanol solution containing 1.64 g of (R)-(-)-mandelic acid was added, and stirred at room temperature for 10 minutes. The residue obtained by concentrating and solidifying methanol, was crystallized with ether, and the crystals were obtained by filtration. The crystals were washed with a small amount of isopropanol and then with ether to obtain 3.2 g of crude crystals. The obtained diastereomer salt was recrystallized with isopropanol to obtain 2.5 g of a salt showing α!D=+6.8(methanol, C=0.49). Further, it was recrystallized with isopropanol to obtain a salt showing α!D=+7.1(methanol, C=0.48). The obtained diastereomer salt was partitioned into 1M aqueous sodium hydroxide solution and dichloromethane, and extracted three times with 10 ml of dichloromethane under alkaline condition. After drying the organic layer, it was concentrated to solidify, an oily free base was obtained. After adding 1 ml of dichloromethane to it, the crystals which were obtained by adding ether containing hydrogen chloride dropwise, were obtained by filtration. The crystals were recrystallized with ethanol to obtain 1.9 g of (2S,3S)-3- (2,2-dimethyl-2,3-dihydrobenzofuran-7-yl)methyl!amino-2-phenylpiperidine hydrochloride.
m.p. 231°-235° C.(dec.); MS 70,161(base),176,217,336(M+); NMR(DMSO-d6) 1.38(3H,s),1.39(3H,s),1.79-1.84(1H,m), 2.11-2.28 (2H,m),2.35-2.40(1H,m),2.97(2H,s),3.13-3.21(1H,m),3.42(1H,d,J=13.6 Hz), 3.43-3.49(1H,m),3.67(1H,d,J=13.6 Hz),3.97(1H,bs),4.99(1H,bs),6.76(1H, t,J=7.5 Hz),7.13-7.21(2H,m),7.43-7.55(3H,m),7.74-7.76(2H,m),9-10(2H,br),10.59(2H,br); Elemental Analysis (C22 H28 N2 O.2HCl); Calculated C:64.54 H:7.39 N:6.84; Found C:64.38 H:7.31 N:6.86
According to the steps described in Reference Example 1--Reference Example 2--Example 1--Example 2, the following compounds were prepared. As to Examples 3, 14, 15 and 22, enantiomers (Reference Examples 3, 4, 5 and 6) of 7-formyl-2-methyl-2,3-dihydrobenzofurans which were prepared based on Reference Example 3, were prepared as raw materials for preparation of epimers derived from mono-methyl group in the 2-position, based on the above steps.
Example 3
(2S,3S)-3- (2-methyl-2,3-dihydrobenzofuran-7-yl)methyl!amino-2-phenylpiperidine hydrochloride
m.p. 228°-231° C.(dec.); MS 70,147(base),162,203,322(M+); NMR(DMSO-d6) 1.33-1.38(3H,m),1.78-1.84(1H,m),2.11-2.44(3H,m), 2.69-2.78(1H,m),3.13-3.48(4H,m),3.69-3.76(1H,m), 3.93-3.99(1H,m),4.81-4.91(1H,m),4.98(1H,bs), 6.76(1H,t,J=7.5 Hz),7.14-7.25(2H,m),7.42-7.53(3H, m),7.72-7.77(2H,m),9-10(2H,br),10.69(2H,br); Elemental Analysis (C21 H26 N2 O.2HCl); Calculated C:63.80 H:7.14 N:7.09; Found C:63.54 H:7.19 N:6.95
Example 3A
(Preparation of epimer 3A from enantiomer A of Reference Example 3)
(2S,3S)-3- (2-methyl-2,3-dihydrobenzofuran-7-yl)methyl!amino-2-phenylpiperidine hydrochloride
m.p. 245°-258° C.(dec.); MS 70,147(base),162,203,322(M+); NMR(DMSO-d6) 1.33(3H,d,J=5.86 Hz); Elemental Analysis (C21 H26 N2 O.2HCl); Calculated C:63.80 H:7.14 N:7.09; Found C:63.84 H:7.20 N:7.14
Example 3B
(Preparation of epimer 3B from enantiomer B of Reference Example 3)
(2S,3S)-3- (2-methyl-2,3-dihydrobenzofuran-7-yl)methyl!amino-2-phenylpiperidine hydrochloride
m.p. 250°-263° C.(dec.); MS 70,147(base),162,203,322(M+); NMR(DMSO-d6) 1.36(3H,d,J=6.22 Hz); Elemental Analysis (C21 H26 N2 O.2HCl); Calculated C:63.80 H:7.14 N:7.09; Found C:63.86 H.7.13 N:7.07
Example 4
(2S,3S)-3- (2,2-dimethyl-5-nitro-2,3-dihydrobenzofuran-7-yl)methyl!amino-2-phenylpiperidine hydrochloride
m.p. 239°-256° C.(dec.); MS 70(base),206,245,262,364,382(M+1); NMR(DMSO-d6) 1.44(3H,s),1.47(3H,s),1.80-1.85(1H,m),2.04-2.26(2H,m),2.37-2.41(1H,m),3.09(2H,s),3.12-3.20(1H, m),3.44(1H,d,J=13.8 Hz),3.43-3.47(1H,m),3.77(1H, d,J=13.8 Hz),3.88(1H,br),4.92(1H,bs),7.47(3H,m), 7.70(2H,m),8.05(1H,d,J=2.4 Hz),8.24(1H,d,J=2.0 Hz), 9-10(2H,br),10.29(2H,br); Elemental Analysis (C22 H27 N3 O3.2HCl); Calculated C:58.15 H:6.43 N:9.25; Found C:58.15 H:6.44 N:9.16
Example 5
(2S,3S)-3- (2,2-dimethyl-5-methylthio-2,3-dihydrobenzofuran-7-yl)methyl!amino-2-phenylpiperidine hydrochloride
m.p. 221°-225° C.(dec.); MS 207(base),263,382(M+); NMR(DMSO-d6) 1.37(3H,s),1.38(3H,s),2.41(3H,s),2.96(2H,s), 1.78-1.84(1H,m),2.04-2.27(2H,m),2.33-2.38(1H,m), 3.12-3.20(1H,m),3.39(1H,d,J=13.9 Hz),3.43-3.49(1H,m),3.66(1H,d,J=13.9 Hz),3.91(1H,bs),4.95(1H, bs),7.12(1H,d,J=1.8 Hz),7.20(1H,d,J=1.8 Hz),7.43-7.55(3H,m),7.71-7.74(2H,m),9-10(2H,br),10.39(2H,br); Elemental analysis (C23 H30 N2 SO.2HCl); Calculated C:60.65 H:7.08 N:6.15; Found C:60.58 H:7.13 N:6.18
Example 6
(2S,3S)-3- (2,2-dimethyl-5-methylsulfonyl-2,3-dihydrobenzofuran-7-yl)methyl!amino-2-phenylpiperidine hydrochloride
m.p. 230°-256° C.(dec.); MS 70(base),175,239,295,414(M+); NMR(DMSO-d6) 1.43(3H,s),1.44(3H,s),1.80-1.85(1H,m),2.07-2.27(2H,m),2.41-2.46(1H,m),3.07(2H,s),3.13(3H,s),3.14-3.21(1H,m),3.39(1H,d,J=13.9 Hz),3.42-3.48(1H,m), 3.76(1H,d=13.9 Hz),3.97(1H,br),4.98(1H,bs),7.43-7.55(3H,m),7.67(1H,d,J=1.8 Hz),7.73-7.76(2H,m), 7.88(1H,d,J=1.8 Hz),9-10(2H,br),10.54(2H,br); Elemental Analysis (C23 H30 N2 SO3.2HCl.0.25H2 O); Calculated C:56.15 H:6.66 N:5.69; Found C:56.09 H:6.68 N:5.78
Example 7
(2S,3S)-3- (2,2-dimethyl-5-dimethylaminosulfonyl-2,3-dihydrobenzofuran-7-yl)methyl!amino-2-phenylpiperidine hydrochloride
m.p. 246°-250° C.(dec.); MS 70(base),175,268,443(M+); NMR(DMSO-d6) 1.43(6H,s),1.79-1.84(1H,m),2.08-2.38(3H,m),2.59(6H,s),3.07(2H,s),3.12-3.20(1H,m),3.41-3.47(1H, m),3.51(1H,d,J=13.9 Hz),3.75(1H,d,J=13.9 Hz),3.84(1H,br),4.91(1H,bs),7.43-7.54(4H,m),7.65-7.71(3H,m),9-10(2H,br),10.21(2H,br); Elemental Analysis (C24 H33 N3 SO3.2HCl); Calculated C:55.81 H:6.83 N:8.14; Found C:55.77 H:6.76 N:8.07
Example 8
(2S,3S)-3- (5-dimethlaminosulfonyl-2-methyl-2,3-dihydrobenzofuran-7-yl)methyl!amino-2-phenylpiperidine hydrochloride
m.p. 236°-240° C.(dec.); MS 70(base),175,254,429(M+); NMR(DMSO-d6) 1.40-1.43(3H,m),1.81-1.91(1H,m),2.08-2.43(3H,m), 2.60(6H,s),2.80-2.89(1H,m),3.13-3.22(1H,m),3.35-3.53(3H,m),3.78-3.85(1H,m),3.91-3.96(1H,m),4.96-5.11(2H,m),7.42-7.53(4H,m),7.69-7.75(3H,m),9-10(2H,br),10.61(2H,br); Elemental Analysis (C23 H31 N3 SO3.2HCl); Calculated C:54.98 H:6.62 N:8.36; Found C:54.98 H:6.73 N:8.36
Example 9
(2S,3S)-3-(3,4-methylenedioxybenzyl)amino-2-phenylpiperidine hydrochloride
m.p. 257°-260° C.(dec.); MS 70,135(base),191,310(M+); NMR(DMSO-d6) 1.79-1.84(1H,m),2.04-2.29(2H,m),2.43(1H,br),3.13-3.21(1H,m),3.25(1H,d,J=13.0 Hz),3.45-3.50(1H,m), 3.63(1H,d,J=13.0 Hz),3.90(1H,bs),4.96(1H,bs),5.99(2H,s),6.67(1H,dd,J=7.9 Hz,J=1.7 Hz),6.83(1H,d, J=7.9 Hz), 6.96(1H,d,J=1.7 Hz),7.45-7.58(3H,m), 7.75-7.78(2H,m), 9.57(2H,br),10.49(2H,br); Elemental Analysis (C19 H22 N2 O2.2HCl); Calculated C:59.54 H:6.31 N:7.31; Found C:59.31 H:6.42 N:7.31
Example 10
(2S,3S)-3- (3,4-dihydro-1,2-benzopyran-8-yl)methyl!amino-2-phenylpiperidine hydrochloride
m.p. 255°-258° C.(dec.); MS 70,147(base),203,322(M+); NMR(DMSO-d6) 1.78-1.90(3H,m),2.09-2.14(1H,m),2.21-2.37(2H, m),2.67(2H,t,J=6.4 Hz),3.13-4.49(2H,m),3,44(1H, d,J=13.0 Hz),3.80(1H,d,J=13.0 Hz),3.90(1H,bs), 3.95-4.13(2H,m),4.93(1H,bs),6.76(1H,t,J=7.6 Hz), 7.04(2H,d,J=7.6 Hz),7.44-7.56(3H,m),7.70-7.73(2H,m),8.2-9.7(2H,br),10.18(2H,br); Elemental Analysis (C21 H26 N2 O.2HCl); Calculated C:63.80 H:7.14 N:7.09; Found C:63.54 H:7.06 N:7.11
Example 11
(2S,3S)-3- (5-chloro-2,2-dimethyl-2,3-dihydrobenzofuran-7-yl)methyl!amino-2-phenylpiperidine hydrochloride
m.p. 220°-231° C.(dec.); α!D=+112.28 (c=0.51, methanol); MS 70(base),195,251,370(M+); NMR(DMSO-d6) 1.34(3H,s),1.38(3H,s),1.70-1.76(1H,m),1.90-2.24(3H,m),2.95(2H,s),3.04-3.64(5H,m),4.73(1H, br),7.14(2H,bs),7.41-7.58(5H,m),8.5-9.5(2H,br), 9.58(2H,br); Elemental Analysis (C22 H27 ClN2 O.2HCl); Calculated C:59.53 H:6.59 N:6.31; Found C:59.31 H:6.57 N:6.37
Example 12
(2S,3S)-3- (2,2-dimethyl-5-methoxy-2,3-dihydrobenzofuran-7-yl)methyl!amino-2-phenylpiperldine hydrochloride
m.p. 207°-216° C.(dec.); MS 70,191(base),206,247,366(M+); NMR(DMSO-d6) 1.35(3H,s),1.36(3H,s),1.78-1.83(1H,m),2.07-2.36(3H,m),2.93(2H,s),3.12-3.21(1H,m), 3.38-3.49(1H,m),3.40(1H,d,J=13.6 Hz),3.66(1H,d,J=13.6 Hz),3.67(3H,s),3.91(1H,br),4.94(1H,bs), 6.77(1H,d,J=2.6 Hz),6.84(1H,d,J=2.6 Hz),7.43-7.55(3H,m),7.71-7.74(2H,m),8.7-9.9(2H,br), 10.27(2H,br); Elemental Analysis (C23 H30 N2 O2.2HCl); Calculated C:62.87 H:7.34 N:6.38; Found C:62.68 H:7.29 N:6.44
Example 13
(2S,3S)-3- (2,3-dihydrobenzofuran-7-yl)methyl!amino-2-phenylpiperidine hydrochloride
m.p. 228°-234° C.(dec.); MS 70,133(base),189,308(M+); NMR(DMSO-d6) 1.76-1.81(1H,m),2.04-2.32(3H,m),3.10-3.49(5H, m),3.75(2H,d,J=13.6 Hz),4.45(2H,t,J=8.8 Hz), 4.87(1H,bs),6.77(1H,t,J=7.5 Hz),7.10-7.19(2H,m), 7.43-7.55(3H,m),7.66-7.69(2H,m),8.3-9.4(2H,br),9.96(2H,br); Elemental Analysis (C20 H24 N2 O.2HCl.1.25H2 O); Calculated C:59.48 H:7.11 N:6.94; Found C:59.67 H:7.03 N:7.07
Example 14
(2S,3S)-3- (5-chloro-2-methyl-2,3-dihydrobenzofuran-7-yl)methyl!amino-2-phenylpiperidine hydrochloride
m.p. 243°-251° C.(dec.); α!D=+56.27 (c=0.51, methanol); MS 70,181(base),237,356(M+); NMR(DMSO-d6) 1.32-1.35(3H,m),1.77-1.82(1H,m),2.04-2.33(3H, m),2.70-2.79(1H,m),3.08-3.48(5H,m),3.69-3.74(1H,m),4.86-4.94(2H,m),7.19-7.25(2H,m),7.42-7.54(3H,m),7.64-7.67(2H,m),8.2-9.8(2H,br),10.01(2H,br); Elemental Analysis (C21 H25 ClN2 O.2HCl); Calculated C:58.68 H:6.33 N:6.52; Found C:58.55 H:6.31 N:6.61
Example 14A
(Preparation of epimer 14A from enantiomer A of Reference Example 4)
(2S,3S)-3- (5-chloro-2-methyl-2,3-dihydrobenzofuran-7-yl)methyl!amino-2-phenylpiperidine hydrochloride
m.p. 228°-242° C.(dec.); MS 70,181(base),237,356(M+); NMR(DMSO-d6) 1.34(3H,d,J=6.23 Hz); Elemental Analysis (C21 H25 ClN2 O.2HCl); Calculated C:58.68 H:6.33 N:6.52; Found C:58.65 H:6.29 N:6.60
Example 14B
(Preparation of epimer 14B from enantiomer B of Reference Example 4)
(2S,3S,)-3- (5-chloro-2-methyl-2,3-dihydrobenzofuran-7-yl)methyl!amino-2-phenylpiperidine hydrochloride
m.p. 249°-261° C.(dec.); MS 70,181(base),237,356(M+); NMR(DMSO-d6) 1.32(3H,d,J=5.86 Hz)); Elemental Analysis (C21 H25 ClN2 O.2HCl); Calculated C:58.68 H:6.33 N:6.52; Found C:58.72 H:6.27 N:6.48
Example 15
(2S,3S)-3- (5-methoxy-2-methyl-2,3-dihydrobenzofuran-7-yl)methyl!amino-2-phenylpiperidine hydrochloride
m.p. 214°-223° C.(dec.); MS 70,177(base),192,233,352(M+); NMR(DMSO-d6) 1.30-1.34(3H,m),1.77-1.82(1H,m),2.06-2.34(3H,m), 2.66-2.75(1H,m),3.12-3.49(4H,m),3.67(3H,s),3.73-3.75(1H,m),3.79-3.93(1H,m),4.74-4.85(1H,m),4.91(1H,bs),6.77-6.84(2H,m),7.43-7.55(3H,m),7.70(2H, br),9-10(2H,br),10.12(2H,br); Elemental Analysis (C22 H28 N2 O2.2HCl); Calculated C:62.12 H:7.11 N:6.59; Found C:62.27 H:7.09 N:6.76
Example 15A
(Preparation of epimer 15A from enantiomer A of Reference Example 5)
(2S,3S)-3- (5-methoxy-2-methyl-2,3-dihydrobenzofuran-7-yl)methyl!amino-2-phenylpiperidine hydrochloride
m.p. 208°-216° C.(dec.); MS 70,177(base),192,233,352(M+); NMR(DMSO-d6) 1.31(3H,d,J=6.23 Hz); Elemental Analysis (C22 H28 N2 O2.2HCl); Calculated C:62.12 H:7.11 N:6.59; Found C:62.09 H:7.13 N:6.64
Example 15B
(Preparation of epimer 15B from enantiomer B of Reference Example 5)
(2S,3S)-3- (5-methoxy-2-methyl-2,3-dihydrobenzofuran-7-yl)methyl!amino-2-phenylpiperidine hydrochloride
m.p. 217°-226° C.(dec.); MS 70,177(base),192,233,352(M+); NMR(DMSO-d6) 1.34(3H,d,J=5.86 Hz); Elemental Analysis (C22 H28 N2 O2.2HCl); Calculated C:62.12 H:7.11 N:6.59; Found C:62.08 H:7.16 N:6.52
Example 16
(2S,3S)-3- 2,2,4-trimethyl-2,3-dihydrobenzofuran-7-yl)methyl!amino-2-phenylpiperidine hydrochloride
m.p. 213°-217° C.(dec.); MS 175(base),350(M+); NMR(CDCl3) 1.27(3H,s),1.32(3H,s),1.55(1H,bs),2.16(3H,s), 2.33(3H,bs),2.84(2H,s),3.17(1H,br),3.38(1H,m), 3.62-3.74(3H,m),5.57(1H,bs),6.57(1H,d,J=7.9 Hz), 6.78(1H,d,J=7.9 Hz),7.36-7.46(H,m),7.69(2H,dd, J=8.1 Hz, J=1.8 Hz),9.85-10.28(2H,br),11.42(2H,br); Elemental Analysis (C23 H30 N2 O.H2 O); Calculated C:62.58 H:7.76 N:6.35; Found C:62.87 H:7.81 N:6.44
Example 17
(2S,3S)-3- (2,2,5-trimethyl-2,3-dihydrobenzofuran-7-yl)methyl!amino-2-phenylpiperidine hydrochloride
m.p. 217°-221° C.(dec.); MS 175(base),350(M+); NMR(DMSO-d6) 1.36(6H,s),1.78-1.83(1H,m),2.17(3H,s),2.08-2.33(3H,m),2.92(2H,s),3.13-3.63(4H,m),3.89(1H, bs),4.93(1H,bs),6.91(1H,s),6.95(1H,s),7.44-7.55(3H,m),7.72(2H,d,J=6.6 Hz),9-10(2H,br), 10.18(2H,br); Elemental Analysis (C23 H30 N2 O.2HCl); Calculated C:65.24 H:7.62 N:6.62; Found C:65.20 H:7.81 N:6.64
Example 18
(2S,3S)-3- (4-chloro-2,2-dimethyl-2,3-dihydrobenzofuran-7-yl)methyl!amino-2-phenylpiperidine hydrochloride
m.p. 216°-225° C.(dec.); MS 195(base),370(M+); NMR(DMSO-d6) 1.42(6H,s),1.78-1.83(1H,m),2.03-2.37(3H,m), 3.01(2H,s),3.12-3.48(3H,m),3.65(1H,d,J=13.6 Hz), 3.89(1H,bs),4.92(1H,bs),6.83(1H,d,J=8.1 Hz), 7.23(1H,d,J=8.1 Hz),7.43-7.54(3H,m),7.71(2H,d, J=6.6 Hz),9-10(2H,br),10.25(2H,br); Elemental Analysis (C22 H27 ClN2 O.2HCl); Calculated C:59.54 H:6.59 N:6.31; Found C:59.72 H:6.60 N:6.46
Example 19
(2S,3S)-3-(3,4-ethylenedioxybenzyl)amino-2-phenylpiperidine hydrochloride
m.p. 231°-244° C.(dec.); MS 149(base),324(M+); NMR(DMSO-d6) 1.79-1.84(1H,m),2.03-2.28(2H,m),2.38-2.43(1H, m),3.13-3.60(4H,m),3.88(1H,bs),4.20(4H,s), 4.95(1H,bs),6.67-6.86(3H,m),7.45-7.56(3H,m), 7.76(2H,d,J=7.0 Hz),9-10(2H,br),10.43(2H,br); Elemental Analysis (C20 H24 N2 O2.2HCl); Calculated C:60.46 H:6.60 N:7.05; Found C:60.46 H:6.62 N:7.10
Example 20
(2S,3S)-3- (2,3-dimethyl-2,3-dihydrobenzofuran-7-yl)methyl!amino-2-phenylpiperidine hydrochloride
m.p. 231°-235° C.(dec.); Ms 161(base),336(M+); NMR(DMSO-d6) 1.24(3H,d,J=6.6 Hz),1.36(3H,d,J=5.9 Hz),1.78-1.83(1H,m),2.03-2.35(3H,m),2.94-3.05(1H,m), 3.12-3.21(1H,m),3.33-3.49(2H,m),3.73-3.78(1H, m),3.87(1H,br),4.25-4.32(1H,m),4.92(1H,bs), 6.76-6.83(1H,m),7.12-7.19(2H,m),7.43-7.55(3H, m),7.71(2H,d,J=6.2 Hz),9-10(2H,br),10.19(2H,br); Elemental Analysis (C22 H28 N2 O.2HCl); Calculated C:64.54 H:7.39 N:6.84; Found D:64.60 H:7.18 N:6.93
Example 21
(2S,3S)-3- (2,3,4-trimethyl-2,3-dihydrobenzofuran-7-yl)methyl!amino-2-phenylpiperidine hydrochloride
m.p. 231°-237° C.(dec.); MS 175(base),350(M+); NMR(DMSO-d6) 0.96-0.99(3H,m),1.33-1.37(3H,m),1.77-1.83(1H, m),1.98-2.38(3H,m),2.22(3H,s),3.01-3.48(4H,m), 3.67-3.72(1H,m),3.89(1H,br),4.62-4.75(1H,m), 4.93(1H,bs),6.60(1H,d,J=8.0 Hz),7.07(1H,dd, J=8.0 Hz,J=1.7 Hz),7.43-7.54(3H,m),7.72-7.74(2H, m),8.7-9.7(2H,br),10.29(2H,br); Elemental Analysis (C23 H30 N2 O.2HCl); Calculated C:65.24 H:7.62 N:6.62; Found C:65.32 H:7.49 N:6.66
Example 22A
(Preparation of epimer 22A from enantiomer A of Reference Example 6)
(2S,3S)-3- (2,5-dimethyl-2,3-dihydrobenzofuran-7-yl)methyl!amino-2-phenylpiperidine hydrochloride
m.p. 228°-245° C.(dec.); MS 70,161(base),336(M+); NMR(DMSO-d6) 1.32(3H,d,J=6.23 Hz); Elemental Analysis (C22 H28 N2 O.2HCl); Calculated C:64.54 H:7.39 N:6.84; Found C:64.51 H:7.38 N:6.91
Example 22B
(Preparation of epimer 22B from enantiomer B of Reference Example 6)
(2S,3S)-3- (2,5-dimethyl-2,3-dihydrobenzofuran-7-yl)methyl!amino-2-phenylpiperidine hydrochloride
m.p. 230°-248° C.(dec.); MS 70,161(base),336(M+); NMR(DMSO-d6) 1.30(3H,d,J=6.23 Hz); Elemental Analysis (C22 H28 N2 O.2HCl); Calculated C:64.54 H:7.39 N:6.84; Found C:64.51 H:7.31 N:6.94
Example 23
(2S,3S)-3- (5-isopropyl-2,3-dihydrobenzofuran-7-yl)methyl!amino-2-phenylpiperidine hydrochloride
m.p. 204°-220° C.(dec.); NMR(DMSO-d6) 1.16(6H,d,J=6.96 Hz, --CH3--(i-Pr)),2.72-2.82(1H, m, --CH═),7.07(2H,s,Ar-H),7.42-7.54(3H,m,Ar-H), 7.72-7.74(2H,m,Ar-H); Elemental Analysis (C23 H30 N2 O.2HCl); Calculated C:65.24 H:7.62 N:6.62; Found C:65.17 H:7.58 N:6.61
Example 24
(2S,3S)-3- (5-tert-butyl-2,3-dihydrobenzofuran-7-yl)methyl!amino-2-phenylpiperidine hydrochloride
m.p. 190°-205° C.(dec.); NMR(DMSO-d6) 1.24(9H,s,t-Bu),7.23(2H,s,Ar-H),7.42-7.54(3H, m,Ar-H),7.73-7.75(2H,m,Ar-H); Elemental Analysis (C24 H32 N2 O.2HCl); Calculated C:65.90 H:7.83 N:6.40; Found C:65.64 H:7.92 N:6.36
Example 25
(2S,3S)-3- (5-cyclopentyl-2,3-dihydrobenzofuran-7-yl)methyl!amino-2-phenylpiperidine hydrochloride
m.p. 194°-201° C.(dec.); NMR(DMSO-d6) 1.45-1.97(8H,m, --CH2--(cyclo-pentyl)),2,79-2.92(1H,m, --CH═),7.07-7.09(2H,m,Ar-H),7.42-7.53(3H, m,Ar-H),7.72-7.75(2H,m,Ar-H); Elemental Analysis (C25 H32 N2 O.2HCl); Calculated C:66.81 H:7.62 N:6.23; Found C:66.15 H:7.59 N:6.19
Example 26
(2S,3S)-3- (5-cyclohexyl-2,3-dihydrobenzofuran-7-yl)methyl!amino-2-phenylpiperidine hydrochloride
m.p. 190°-205° C.(dec.); NMR(DMSO-d6) 1.17-1.43(5H,m, --CH2--(cyclo-hexyl)),1.68-1.83(5H,m, --CH2--(cyclo-hexyl)),7.04(2H,s,Ar-H), 7.42-7.54(3H,m,Ar-H),7.71-7.73(2H,m,Ar-H); Elemental Analysis (C26 H34 N2 O.2HCl.0.25H2 O); Calculated C:66.73 H:7.86 N:5.99; Found C:66.83 H:7.85 N:5.98
Example 27
(2S,3S)-3- (5-ethylthio-2,3-dihydrobenzofuran-7-yl)methyl!amino-2-phenylpiperidine hydrochloride
m.p. 206°-227° C.(dec.); NMR(DMSO-d6) 1.18(3H,t,J=7.33 Hz,CH3--),2.86(2H,q,J=7.33 Hz), --CH2--),7.20(1H,s,Ar-H),7.27(1H,s,Ar-H),7.42-7.53(3H,m,Ar-H),7.73-7.74(2H,m,Ar-H); Elemental Analysis (C22 H28 N2 OS.2HCl); Calculated C:59.86 H:6.85 N:6.35; Found C:59.92 H:6.87 N:6.23
Example 28
(2S,3S)-3- (5-isopropylthio-2,3-dihydrobenzofuran-7-yl)methyl!amino-2-phenylpiperidine hydrochloride
m.p. 188°-198° C.(dec.); NMR(DMSO-d6) 1.19(6H,d,7.33 Hz, --CH3--(i-Pr)),3,20-3.30(1H,m, --CH═),7.23-7.30(2H,m,Ar-H),7.42-7.54(3H,m,Ar-H), 7.69-7.72(2H,m,Ar-H); Elemental Analysis (C23 H30 N2 OS.2HCl); Calculated C:60.65 H:7.08 N:6.15; Found C:60.50 H:7.08 N:6.04
Example 29
(2S,3S)-3- (5-cyclohexylthio-2,3-dihydrobenzofuran-7-yl)methyl!amino-2-phenylpiperidine hydrochloride
m.p. 203°-220° C.(dec.); NMR(DMSO-d6) 1.06-1.37(5H,m,cyclo-pentyl),1.52-1.91(6H,m, cyclo-pentyl),7.22(1H,s,Ar-H),7.31(1H,s,Ar-H), 7.42-7.53(3H,m,Ar-H),7.72-7.73(2H,m,Ar-H); Elemental Analysis (C26 H34 N2 OS.2HCl); Calculated C:63.02 H:7.33 N:5.65; Found C:63.09 H-7.36 N:5.58
Example 30
(2S,3S)-3- (5-trifluoromethylthio-2,3-dihydrobenzofuran-7-yl)methyl!amino-2-phenylpiperidine hydrochloride
m.p. 205°-215° C.(dec.); NMR(DMSO-d6) 3.17-3.24(2H,m, --CH2),4.55-4.62(2H,m, --CH2--), 7.42-7.53(3H,m,Ar-H),7.61(1H,s,Ar-H),7.69-7.71(2H,m,Ar-H); Elemental Analysis (C21 H23 F3 N2 OS.2HCl); Calculated C:52.40 H:5.23 N:5.82; Found C:52.55 H:5.22 N:5.78
Example 31
(2S,3S)-3- (5-(2,2,2-trifluoroethyl)thio-2,3-dihydrobenzofuran-7-yl)methyl!amino-2-phenylpiperidine hydrochloride
m.p. 197°-205° C.(dec.); NMR(DMSO-d6) 3.83(2H,q,J=10.26 Hz, --CH2CF3--),7.35-7.36(1H,m, Ar-H),7.42-7.53(4H,m,Ar-H),7.71-7.74(2H,m,Ar-H); Elemental Analysis (C22 H25 F3 N2 OS.2HCl); Calculated C:53.34 H:5.49 N:5.65; Found C:53.35 H:5.52 N:5.57
Example 32
(2S,3S)-3- (5-methylsulfinyl-2,3-dihydrobenzofuran-7-yl)methyl!amino-2-phenylpiperidine hydrochloride
m.p. 221°-244° C.(dec.); NMR(DMSO-d6) 2.69(3H,s,CH3--),7.42-7.72(7H,m,Ar-H); Elemental Analysis (C21 H26 N2 OS.2HCl); Calculated C:59.01 H:6.60 N:6.55; Found C:59.12 H:6.31 N:6.64
Example 33
(2S,3S)-3- (5-isopropylsulfonyl-2,3-dihydrobenzofuran-7-yl)methyl!amino-2-phenylpiperidine hydrochloride
m.p. 188°-197° C.(dec.); NMR(DMSO-d6) 1.13-1.16(6H,d,J=6.23 Hz, --CH3(i-Pr)),3,28-3.38(1H,m, --CH═(i-Pr)),7.42-7.54(3H,m,Ar-H),7.62-7.63(1H,m,Ar-H),7.70-7.74(3H,m,Ar-H); Elemental Analysis (C23 H30 N2 O3 S.2HCl); Calculated C:64.54 H:7.39 N:6.84; Found C:64.51 H:7.31 N:6.94
Example 34
(2S,3S)-3- (5-isopropylsulfonyl-2-methyl-2,3-dihydrobenzofuran-7-yl)methyl!amino-2-phenylpiperidine hydrochloride
m.p. 215°-241° C.(dec.); NMR(DMSO-d6) 1.14(6H,d,J=6.96 Hz, --CH3(i-Pr))),4.99-5.10(1H,m, --CH═(i-Pr)),7.43-7.76(7H,m,Ar-H); Elemental Analysis (C24 H32 N2 O3 S.2HCl); Calculated C:57.48 H:6.83 N:5.59; Found C:57.71 H:6.56 N:5.38
Example 35
(2S,3S)-3- (5-cyclopentylsulfonyl-2,3-dihydrobenzofuran-7-yl)methyl!amino-2-phenylpiperidine hydrochloride
m.p. 212°-225° C.(dec.); NMR(DMSO-d6) 1.50-1.91(8H,m, --CH2--(cyclo-pentyl)),3.63-3.75(1H,m, --CH═(cyclo-pentyl)),7.42-7.54(3H,m,Ar-H), 7.65-7.77(4H,m,Ar-H); Elemental Analysis (C25 H32 N2 O3 S.2HCl); Calculated C:58.47 H:6.67 N:5.46; Found C:58.10 H:6.65 N:5.34
Example 36
(2S,3S)-3- (2-methyl-5-methylaminosulfonyl-2,3-dihydrobenzofuran-7-yl)methyl!amino-2-phenylpiperidine hydrochloride
m.p. 253°-275° C.(dec.); NMR(DMSO-d6) 1.40-1.42(3H,m,CH3--),2.40(3H,s,CH3--),7.43-7.75(7H,m); Elemental Analysis (C22 H29 N3 O3 S.2HCl); Calculated C:54.10 H:6.40 N:8.60; Found C:54.31 H:6.31 N:8.84
Example 37
(2S,3S)-3- (5-methoxy-2,3-dihydrobenzofuran-7-yl)methyl!amino-2-phenylpiperidine hydrochloride
m.p. 260° C.(dec.); NMR(DMSO-d6) 3.68(3H,s, --OCH3),6.81-6.85(2H,m,Ar-H),7.42-7.55(3H,m,Ar-H),7.71-7.73(2H,m,Ar-H); Elemental Analysis (C21 H26 N2 O2.2HCl.0.5H2 O); Calculated C:60.00 H:6.95 N:6.66; Found C:60.23 H:6.98 N:6.56
Example 38
(2S,3S)-3- (2,2-dimethyl-5-fluoro-2,3-dihydrobenzofuran-7-yl)methyl!amino-2-phenylpiperidine hydrochloride
m.p. 227°-237° C.(dec.); NMR(DMSO-d6) 1.375(3H,s, --CH3),1.379(3H,s, --CH3),2.98(2H,s, --CH2),6.99-7.14(2H,m,Ar-H(F)),7.43-7.54(3H,m, Ar-H),7.71-7.73(2H,m,Ar-H); Elemental Analysis (C22 H27 FN2 O.2HCl); Calculated C:61.83 H:6.84 N:6.55; Found C:61.77 H:6.86 N:6.56
Example 39
(2S,3S)-3- (5-hydroxy-2-methyl-2,3-dihydrobenzofuran-7-yl)methyl!amino-2-phenylpiperidine hydrochloride
m.p. 195° C.(dec.); NMR(DMSO-d6) 1.29-1.34(3H,m, --CH3),4.71-4.82(1H,m, --CH═), 6.54-6.65(2H,m,Ar-H(OH)),7.43-7.55(3H,m,Ar-H), 7.71-7.75(2H,m,Ar-H); Elemental Analysis (C21 H26 FN2 O2.2HCl.H2 O); Calculated C:58.74 H:7.04 N:6.52; Found C:58.85 H:7.47 N:6.31
Example 40
(2S,3S)-3- (5-fluoro-2-methyl-2,3-dihydrobenzofuran-7-yl)methyl!amino-2-phenylpiperidine hydrochloride
m.p. 220°-230° C.(dec.); NMR(DMSO-d6) 1.33-1.37(3H,m, --CH3),4.83-4.93(1H,m, --CH═), 7.00-7.21(2H,m,Ar-H(F)),7.42-7.53(3H,m,Ar-H), 7.71-7.75(2H,m,Ar-H); Elemental Analysis (C21 H25 FN2 O.2HCl); Calculated C:61.02 H:6.58 N:6.78; Found C:60.63 H:6.48 N:6.50
Example 41
(2S,3S)-3- (5-nitro-2,3-dihydrobenzofuran-7-yl)methyl!amino-2-phenylpiperidine hydrochloride
m.p. 240°-250° C.(dec.); NMR(DMSO-d6) 3.23-3.29(2H,m, --CH2--),4.66-4.73(2H,m, --CH2--), 7.41-7.53(3H,mAr-H),7.70-7.73(2H,m,Ar-H), 8.08(1H,d,2,2 Hz,Ar-H(--NO2)),8.26(1H,d,2,2 Hz, Ar-H(--NO2)); Elemental Analysis (C20 H23 N3 O3.2HCl); Calculated C:56.34 H:5.91 N:9.86; Found C:55.91 H:5.98 N:9.53
Example 42
(2S,3S)-3- (2-methyl-5-methylsulfonyl-2,3-dihydrobenzofuran-7-yl)methyl!amino-2-phenylpiperidine hydrochloride
m.p. 225°-250° C.(dec.); NMR(DMSO-d6) 1.39-1.42(3H,m,CH3--),3,12(3H,s,CH3--),7.43-7.86(7H,m,Ar-H); Elemental Analysis (C22 H28 N2 O3 S.2HCl); Calculated C:55.81 H:6.39 N:5.92; Found C:55.76 H:6.23 N:5.73
Example 43
(2S,3S)-3- 2-methyl-5-methylthio-2,3-dihydrobenzofuran-7-yl)methyl!amino-2-phenylpiperidine hydrochloride
m.p. 225°-240° C.; NMR(DMSO-d6) 1.31-1.35(3H,m,CH3--),2,50(3H,s,CH3--),7.13-7.68(7H,m,Ar-H); Elemental Analysis C22 H28 N2 OS.2HCl); Calculated C:59.86 H:6.85 N:6.35; Found C:59.60 H:7.00 N:6.06
Example 44
(2S,3S)-3- (5-dimethylaminosulfonyl-2,3-dihydrobenzofuran-7-yl)methyl!amino-2-phenylpiperidine hydrochloride
m.p. 236°-250° C.(dec.); NMR(DMSO-d6) 2.60(6H,s,(CH3)2),7.42-7.72(7H,m,Ar-H); Elemental Analysis (C22 H29 N3 O3 S.2HCl); Calculated C:54.10 H:6.40 N:8.60; Found C:53.85 H:6.40 N:8.44
Example 45
(2S,3S)-3- (5-methylsulfonyl-2,3-dihydrobenzofuran-7-yl)methyl!amino-2-phenylpiperidine hydrochloride
m.p. 240°-250° C.(dec.); NMR(DMSO-d6) 3.12(3H,s,CH3--),7.42-7.54(3H,m,Ar-H),7.68-7.80(4H,m,Ar-H); Elemental Analysis (C21 H26N2 O3 S.2HCl); Calculated C:54.90 H:6.14 N:6.10; Found C:54.23 H:6.07 N:5.68
Example 46
(2S,3S)-3- (5-methylthio-2,3-dihydrobenzofuran-7-yl)methyl!amino-2-phenylpiperidine hydrochloride
m.p. 235°-260° C.(dec.); NMR(DMSO-d6) 2.42(3H,s,CH3--),7.17(1H,s,Ar-H),7.19(1H,s,Ar-H), 7.42-7.54(3H,m,Ar-H),7.70-7.72(2H,m,Ar-H); Elemental Analysis (C21 H26 N2 OS.2HCl); Calculated C:59.01 H:6.60 N:6.55; Found C:59.06 H:6.60 N:6.27
Example 47
(2S,3S)-3- (5-methyl-2,3-dihydrobenzofuran-7-yl)methyl!amino-2-phenylpiperidine hydrochloride
m.p. 230°-250° C.(dec.); NMR(DMSO-d6) 2.18(3H,s,CH3),6.98(1H,s,Ar-H),7.00(1H,s,Ar-H), 7.42-7.54(3H,m,Ar-H),7.72-7.75(2H,m,Ar-H); Elemental Analysis (C21 H26 N2 O.2HCl.H2 O); Calculated C:61.02 H:7.31 N:6.78; Found C:61.37 H:7.47 N:6.70
Example 48
(2S,3S)-3- (5-chloro-2,3-dihydrobenzofuran-7-yl)methyl!amino-2-phenylpiperidine hydrochloride
m.p. 260°-263° C.(dec.); NMR(DMSO-d6) 3.12-3.18(2H-,m, --HC2--),4.47-4.54(2H,m, --CH2--), 7.23-7.29(2H,m,Ar-H(Cl)),7.42-7.54(3H,m,Ar-H), 7.69-7.71(2H,m,Ar-H); Elemental Analysis (C20 H23 N2 OCl.2HCl); Calculated C:57.77 H:6.06 N:6.74; Found C:57.92 H:6.14 N:6.56
Example 49
(2S,3S)-3- (5-ethoxy-2-methyl-2,3-dihydrobenzofuran-7-yl)methyl!amino-2-phenylpiperidine hydrochloride
m.p. 190°-194° C.(dec.); NMR(DMSO-d6) 1.19-1.35(6H,m, --CH3),3.89-3.97(2H,q, --CH2--), 4.75-4.85(1H,m, --CH═),6.75-6.87(2H,m,Ar-H), 7.42-7.54(3H,m,Ar-H),7.71-7.74(2H,m,Ar-H); Elemental Analysis (C23 H30 N2 O2.2HCl); Calculated C:62.87 H:7.34 N:6.38; Found C:62.46 H:7.37 N:6.23
Example 50
(2S,3S)-3- (5-cyclopentyloxy-2-methyl-2,3-dihydrobenzofuran-7-yl)methyl!amino-2-phenylpiperidine hydrochloride
m.p. 182°-188° C.(dec.); NMR(DMSO-d6) 1.30-1.35(3H,m, --CH3),1.53-1.86(8H,m, --CH2--(cyclopentyl)), 4.63-4.84(2H,m, --CH═*2),6.72-6.82 (2H,m,Ar-H),7.42-7.53(3H,m,Ar-H),7.70-7.73(2H,m,Ar-H); Elemental Analysis (C26 H34 N2 O2.2HCl); Calculated C:65.13 H:7.57 N:5.84; Found C:64.83 H:7.81 N:5.52
Example 51
(2S,3S)-3- (2,4-dimethyl-5-dimethylaminosulfonyl-2,3-dihydrobenzofuran-7-yl)methyl!amino-2-phenylpiperidine hydrochloride
m.p. 221°-231° C.(dec.); NMR(DMSO-d6) 1.39-1.43(3H,m, --CH3),2,37(3H,s, --CH3),2.67(6H, s,N,N-dimethyl),4.98-5.08(1H,m, --CH═),7.43-7.52(3H,m,Ar-H),7.67-7.70(3H,m,Ar-H); Elemental Analysis (C25 H34 N2 O2.2HCl); Calculated C:55.81 H:6.83 N:8.14; Found C:55.78 H:6.86 N:8.02
Example 52
(2S,3S)-3- (2-methyl-5-(1-pyrrolidinyl)sulfonylamino-2,3-dihydrobenzofuran-7-yl)methyl!amino-2-phenylpiperidine hydrochloride
m.p. 215°-224° C.(dec.); NMR(DMSO-d6) 1.39-1.42(3H,m, --CH3),1.64-1.69(4H,m, --CH2--), 4.96-5.07(1H,m, --CH═),7.46-7.57(4H,m,Ar-H), 7.70-7.73(3H,m,Ar-H); Elemental Analysis (C25 H33 N3 O3 S.2HCl); Calculated C:56.81 H:6.67 N:7.95; Found C:56.41 H:6.79 N:7.68
Example 53
(2S,3S)-3- (5-trifluoromethoxy-2,3-dihydrobenzofuran-7-yl)methyl!amino-2-phenylpiperidine hydrochloride
m.p. 240°-270° C.(dec.); NMR(DMSO-d6) 7.21(1H,s,Ar-H),7.26(1H,s,Ar-H),7.42-7.68(3H, m,Ar-H),7.70-7.71(2H,m,Ar-H); Elemental Analysis (C21 H23 N2 O2 F3.2HCl); Calculated C:54.20 H:5.41 N:6.02; Found C:54.20 H:5.52 N:5.89
Formulation Examples
Hereinafter, Formulation Examples of the compounds of the present invention will be described.
Formulation Example 1 (Tablets)
______________________________________
(1)Compound of Example 46
                    5
(2)Lactose         55
(3)Crystalline cellulose
                   18
(4)Cornstarch      18
(5)Hydroxypropyl cellulose
                    3
(6)Magnesium stearate
                    1
                   100(%(w/w))
______________________________________
The above components (1) to (5) were mixed sufficiently. Water was added to the mixture, and the mixture was granulated. Then, after drying and sizing the obtained granules, the (6) was added and mixed. These mixtures were compression-molded to formulate tables each containing 100 mg of an effective component.
Formulation Example 2 (Tablets)
______________________________________
(1)Compound of Example 37
                   20
(2)Fumaric acid    10
(3)Calcium phosphate
                   45
(4)Lactose         24
(5)Talc             1
                   100(%(w/w))
______________________________________
On the tablets which were prepared in the same manner as described in Formulation Example 1 using the above-components (1) to (5), a coating solution comprising ethyl cellulose, polyvinyl pyrrolidone K30, talc and ethyl alcohol was spray-coated in the conventional method so as to obtain a sustained-release formulation.
Formulation Example 3 (Capsules)
______________________________________
(1)Compound of Example 23
                    8
(2)Lactose         66
(3)Corn starch     21
(4)Hydroxypropyl cellulose
                     3.5
(5)Light silicic anhydride
                     0.5
(6)Magnesium stearate
                    1
                   100(%(w/w))
______________________________________
After mixing the above-components (1) to (6) and making into granules in the conventional method, the granules were filled into a capsule to prepare a capsule containing 100 mg of the compound of the present invention.
Formulation Example 4 (Formulation for parenteral administration)
______________________________________
(1)Compound of Example 30
                         3.0    g
(2)Soybean oil, Pharmacopoeia Japonica
                         20.0   g
(3)Purified soybean phospholipid
                         2.5    g
(4)Glycerine             5.0    g
(5)Distilled water       175    ml
______________________________________
The above-component (1) was dissolved in the (4) and (5), previously. The oil component, in which the (2) and (3) were mixed, was added to the solution, and mixed sufficiently to prepare a formulation for parenteral administration of fat emulsion.
Formulation Example 5 (Formulation for parenteral administration)
______________________________________
(1)Compound of Example 31
                        2.0    g
(2)Glycerine            40.0   g
(3)Distilled water      100    mg
______________________________________
The above-component (1) was added to (2) and (3), and mixed sufficiently to prepare an aqueous formulation for parenteral administration.
Formulation Example 6 (Ointments)
______________________________________
(1)Compound of Example 3
                   3.0%(w/w)
(2)Propylene glycol
                   6.5%(w/w)
(3)Isopropyl myristate
                   5.5%(w/w)
(4)White vaseline 85.0%(w/w)
                   100%(w/w)
______________________________________
An ointment was prepared in the conventional method using the above-components (1) to (4).
Formulation Example 7 (Liniments)
______________________________________
(1)Compound of Example 5
                      1.0%(w/w)
(2)Ethanol           38.0%(w/w)
(3)2-hydroxy-4-methoxybenzophenone
                      0.5%(w/w)
(4)Propylene glycol  13.0%(w/w)
(5)Methyl cellulose   0.8%(w/w)
(6)Ethyl sebacate     3.0%(w/w)
(7)Purified water    suitable amout
(8)Sodium hydroxide   0.7%(w/w)
                      100%(w/w)
______________________________________
Using the above-components (1) to (8), a liniment was prepared in the conventional method.
Formulation Example 8 (Ointments)
______________________________________
(1)Compound of Example 14
                          1.0%(w/w)
(2)White vaseline        78.0%(w/w)
(3)Isopropyl myristate   12.0%(w/w)
(4)Spermaceti             6.0%(w/w)
(5)Polyoxyethylene lauryl ether sodium phosphate
                          3.0%(w/w)
                          100%(w/w)
______________________________________
Using the above-components (1) to (5), an ointment was prepared in the conventional method.
Formulation Example 9 (Gels)
______________________________________
(1)Compound of Example 17
                    3.0%(w/w)
(2)Diisopropyl adipate
                    3.0%(w/w)
(3)Ethanol         38.5%(w/w)
(4)Carboxy vinyl polymer
                    2.0%(w/w)
(5)Purified water  suitable amount
(6)Hydroxypropyl cellulose
                    2.0%(w/w)
(7)Propylene glycol
                   17.0%(w/w)
(8)Diisopropanol amine
                    2.5%(w/w)
                    100%(w/w)
______________________________________
Using the above-components (1) to (8), a gel was prepared by the conventional method.
Formulation Example 10 (Gel creams)
______________________________________
(1)Compound of Example 25
                       1.0%(w/w)
(2)Isopropyl myristate
                      11.0%(w/w)
(3)Ethanol             6.0%(w/w)
(4)Carboxy vinyl polymer
                       1.5%(w/w)
(5)Purified water     Suitable amount
(6)Polyoxyethylene (55) monostearate
                       1.0%(w/w)
(7)Coconut oil fatty acid diethanol amide
                       4.0%(w/w)
                       100%(w/w)
______________________________________
Using the above-components (1) to (7), a gel cream was prepared in the conventional method.
Formulation Example 11 (Suppositories)
______________________________________
(1)Compound of Example 23
                       3.0%(w/w)
(2)Polyethylene glycol
                       6.0%(w/w)
(3)Bleached beeswax   10.0%(w/w)
(4)Sorbitan sesquioleate
                      4.49%(w/w)
(5)Middle-chain fatty acid triglyceride
                      76.5%(w/w)
(6)Dibutyl hydroxy toluene
                      0.01%(w/w)
                       100%(w/w)
______________________________________
Using the above-components (1) to (6), suppositories were prepared in the conventional method.
Formulation Example 12 (Poultices)
______________________________________
(1)Compound of Example 24
                   3.0%(w/w)
(2)Gelatin         9.0%(w/w)
(3)Aluminum silicate
                  11.0%(w/w)
(4)Polyvinyl alcohol
                   4.5%(w/w)
(5)Purified water suitably amount
(6)Glycerine      28.0%(w/w)
(7)Carboxymethyl cellulose
                   3.0%(w/w)
                   100%(w/w)
______________________________________
Using the above-components (1) to (7), a poultice was prepared in the conventional method.
Formulation Example 13 (Plasters)
______________________________________
(1)Compound of Example 46
                        3.0%(w/w)
(2)Styrene-isoprene-styrene block copolymer
                       24.0%(w/w)
(Califlex TR1107; Shell Chemical)
(3)Liquid paraffin     43.5%(w/w)
(4)Hydrogenated rosin ester
                       29.0%(w/w)
                        100%(w/w)
______________________________________
Using the above-components (1) to (4), a plaster was prepared by the conventional method.
Test Examples
Hereinafter, the receptor-binding test (A), the bioassay test using guinea pig ileum (B), the antagonism test on Substance P-induced air way edema (C), and the anti-emetic test (D) to cisplatin-induced emesis and toxicity test (E) of the compounds of the present invention, will be shown.
A. Receptor-Binding Test
The test was carried out based on the method described in Y. Shimohigashi, H. Matsumoto, Y. Takano et al., Biochem.Biophys.Res.Commun., 193(No.2),624-630(1993)).
After exsanguinating guinea pigs deadly, ileum was removed and the longitudinal muscle was stripped off in ice-cold Krebes solution (127 mM NaCl, 2.2 mM KCl, 1.8 mM CaCl2, 25 mM NaHCO3 and 10 mM glucose). To the longitudinal muscles, 20 times of the wet weight of the buffer solution (1) (50 mM tris-HCl buffer solution containing 2 mM MgCl2 and 0.1 mM phenyl methyl sulfonyl-fluoride, pH 7.4) was added. The mixture was homogenized under ice-cooling and centrifuged at 48,000×G for 15 minutes. After removing the supernatant, the pellets were re-suspended in the buffer solution (1) and centrifuged at 48,000×G for 15 minutes. The buffer solution (2) (50 mM tris.HCl buffer solution containing 10 mM ethylenediaminetetraacetic acid and 300 mM KCl, pH 7.4) was added to the pellets and suspended to be reacted under ice-cooling for 60 minutes. The resulted reaction materials were centrifuged at 48,000×G for 15 minutes. After suspending the pellets in the buffer solution (1) and distributing, the mixture were centrifuged at 48,000×G for 15 minutes. The pellets were stored at -80° C. until used as receptor samples.
Thus obtained receptor samples were suspended in 50 mM tris-HCl buffer solution to be used. As the buffer solution, binding buffer solution (tris.HCl buffer solution containing 0.02% bovine serum albumin, 40 μg/ml bacitracin, 4 μg/ml chymostatin, 4 μg/ml leupeptin and 3 mM MnCl2, pH7.4) was used. As the reaction conditions, 125 I!SP50pM was used as a ligand, and the reaction temperature and time were at 22° C. and for 20 minutes. The results will be shown in Table 1.
B. Bioassay Test
The test was carried out based on the method described in Hiroshi Morimoto, Masako Murai, Yasue Maeda et al., J.Pharmacol.Exp.Ther., 262(No.1),398-402(1992)).
After exsanguinating guinea pigs (body weight: 500-600 g) deadly, ileum was removed and 2 cm of ileum strips were prepared. In a Tyrode's solution (10 ml, 37° C.) in which air is passed, containing 5.2 μM atropine and 4.1 μM indomethacin, the strips having 0.5 g resting tension was suspended, and contractions of muscle were recorded on a recording device (RTA-1200, manufactured by Nihon Kohden) via an isotonic transducer (TB-612T, manufactured by Nihon Kohden). Using three specimens per one group, effects of the subject drugs on the muscle contraction caused by 10-8 M Substance P were determined. The muscle contraction caused by Substance P was regarded as 100%, and inhibition rates % with 10-7 M drugs were determined. The results will be shown in Table 1.
Test 1 
______________________________________
            Binding Inhibition
                          Contriction Inhibition
Subject Compound
            (%)           (%)
(Example No.)
            (10.sup.-8  M)
                          (10.sup.-7  M)
______________________________________
2           74.8          47.0
3           96.0          93.2
4           89.7          60.2
5           91.8          80.5
6           74.8          50.9
7           54.0          15.0
8           92.0          85.0
9           36.6           5.5
10          86.2          61.8
11          85.8          58.2
12          82.2          43.0
13          84.7          47.4
14          93.5          92.3
15          88.1          75.2
16          82.5          78.3
17          94.2          94.6
18          89.9          81.2
19          48.7          22.1
20          65.0          38.9
21          53.1          13.4
23          83.2          80.3
24          50.3          69.5
25          89.2          85.1
26          56.4          62.1
46          65.3          72.3
53          53.5          69.3
______________________________________
As clear from the results shown in table 1, it is proved that the piperidine derivatives of the present invention have a very high antagonism on Substance P in the receptor-binding test and bioassay test.
C. Antagonism Test on Substance P-induced Airway Edema
20 mg/kg of Evans' Blue and 1 nm/kg Substance P containing 200 I.U./kg of heparin were administered intravenously to hartley male guinea pigs in order to induce airway edema. After ten minutes, the guinea pigs were exsanguinated deadly. The amounts of the dye transudated into trachea and main bronchi were determined. 1 mg/kg of the subject compounds were administered orally at thirty minutes before the induction. The results will be shown in Table 2 as the inhibition rates compared to the control group. Further, for comparison, the following compounds A and B were used.
Compound A: (2S,3S)-3-(2-methoxybenzyl)amino-2-phenylpiperidine hydrochloride
Compound B: (2S,3S)-3-(2-methoxy-5-trifluoromethoxybenzyl)amino-2-phenylpiperidine hydrochloride
              TABLE 2
______________________________________
Subject Compound
                Inhibition Rate
(Example No.)   (%)
______________________________________
23              89
24              64
25              90
26              61
46              72
53              69
Compound A      12
(10 mg/kg)
Compound B      44
(1 mg/kg)
______________________________________
From the results shown in Table 2, the compounds of the present invention have a very high antagonism on Substance P.
D. Anti-emetic Effect against Cisplatin-induced Emesis
The test was carried out using male ferret (approx. 1.5 kg.). Emesis was induced by intraperitoneal administration of cisplatin (10 mg/kg). 1 mg/kg of the subject compounds were administered orally just after the cisplatin administration. The results will be shown in Table 3 as the inhibition rates compared to the control group, using the number of vomits as indexes. Further, for comparisons, the following compounds A and C were used.
Compound A: (2S,3S)-3-(2-methoxybenzyl)amino-2-phenylpiperidine hydrochloride
Compound C: (2S,3S)-N-(5-isopropyl-2-methoxyphenyl)methyl-1-azabicyclo 2,2,2!octane-3-amine hydrochloride
              TABLE 3
______________________________________
Subject Compound
                Inhibition Rate
(Example No.)   (%)
______________________________________
23              70
25              73
46              60
53              65
Compound A      19
(10 mg/kg)
Compound C      10
(1 mg/kg)
______________________________________
From the results shown in Table 3, it is proved that the compounds of the present invention have a very high anti-emetic effect.
E. Toxicity Test
3, 10 and 30 mg/kg of the compound of Example 46 are administered to five male SD rats per one group for seven days. The compound had no influence on body weights gains, organ weights, numbers of erythrocytes nor numbers of leukocytes.
Industrial Applicability
The piperidine derivatives of the present invention have a distinguished antagonism on Substance P. The piperidine derivatives of the present invention, therefore, are expected to be used as a preventive or remedy for a variety of diseases mediated by Substance P and are useful for pharmaceutical industries.

Claims (15)

We claim:
1. A piperidine compound selected from formula (I): ##STR6## or pharmaceutically acceptable acid addition salts thereof: wherein n represents an integer of 0 or 1; X represents CH2, O or CH--CH3 ; R represents hydrogen, halogen, lower alkyl, hydroxy, lower alkoxy, lower alkylthio, lower alkylsulfinyl, lower alkylsulfonyl, substituted aminosulfonyl or nitro; R1 and R2 may be the same or different and each represents hydrogen or lower alkyl.
2. A cis-piperidine compound selected from formula (Ia): ##STR7## or pharmaceutically acceptable acid addition salts thereof; wherein n represents an integer of 0 or 1; X represents CH2, O or CH--CH3 ; R represents hydrogen, halogen, lower alkyl, hydroxy, lower alkoxy, lower alkylthio, lower alkylsulfinyl, lower alkylsulfonyl, substituted aminosulfonyl or nitro; R1 and R2 may be the same or different and each represents hydrogen or lower alkyl.
3. A cis-piperidine compound selected from formula (Ib): ##STR8## or pharmaceutically acceptable acid addition salts thereof: wherein R represents hydrogen, halogen, lower alkyl, hydroxy, lower alkoxy, lower alkylthio, lower alkylsulfinyl, lower alkylsulfonyl, substituted aminosulfonyl or nitro; R1 and R2 may be the same or different and each represents hydrogen or lower alkyl.
4. A pharmaceutical composition comprising a substance P antagonistic effective amount of a piperidine compound or pharmaceutically acceptable acid addition salt thereof as claimed in claim 1 together with a pharmaceutically acceptable carrier.
5. A pharmaceutical composition comprising a substance P antagonistic effective amount of a piperidine compound or pharmaceutically acceptable acid addition salt thereof as claimed in claim 2 together with a pharmaceutically acceptable carrier.
6. A pharmaceutical composition comprising a substance P antagonistic effective amount of a piperidine compound or pharmaceutically acceptable acid addition salt thereof as claimed in claim 3 together with a pharmaceutically acceptable carrier.
7. The pharmaceutical composition of claim 4 which is for oral, parenteral, intrarectal or percutaneous administration.
8. The pharmaceutical composition of claim 5 which is for oral, parenteral, intrarectal or percutaneous administration.
9. The pharmaceutical composition of claim 6 which is for oral, parenteral, intrarectal or percutaneous administration.
10. A method of treating or preventing asthma comprising administering to a subject in need thereof, a substance P antagonistic effective amount of a piperidine compound or pharmaceutically acceptable acid addition salt thereof as claimed in claim 1.
11. A method of treating or preventing asthma comprising administering to a subject in need thereof, a substance P antagonistic effective amount of a piperidine compound or pharmaceutically acceptable acid addition salt thereof as claimed in claim 2.
12. A method of treating or preventing asthma comprising administering to a subject in need thereof, a substance P antagonistic effective amount of a piperidine compound or pharmaceutically acceptable acid addition salt thereof as claimed in claim 3.
13. A method of treating or preventing emesis comprising administering to a subject in need thereof, a substance P antagonistic effective amount of a piperidine compound or pharmaceutically acceptable acid addition salt thereof as claimed in claim 1.
14. A method of treating or preventing emesis comprising administering to a subject in need thereof, a substance P antagonistic effective amount of a piperidine compound or pharmaceutically acceptable acid addition salt thereof as claimed in claim 2.
15. A method of treating or preventing emesis comprising administering to a subject in need thereof, a substance P antagonistic effective amount of a piperidine compound or pharmaceutically acceptable acid addition salt thereof as claimed in claim 3.
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Cited By (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US6239147B1 (en) * 1999-05-21 2001-05-29 Pfizer Inc 1-trifluoromethyl-4-hydroxy-7-piperidinyl-aminomethylchroman derivatives
US20030152626A1 (en) * 1998-05-26 2003-08-14 Steffen Lang New pharmaceutical compositions
US7235257B1 (en) * 1999-12-14 2007-06-26 Rohto Pharmaceutical Co., Ltd. Drugs for relieving hemicrania comprising 1-menthol and essential oils
US20070218143A1 (en) * 2006-03-20 2007-09-20 Chong Mok T M Topical preparation

Families Citing this family (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
TW426667B (en) * 1997-11-19 2001-03-21 Pfizer Piperidinylaminomethyl trifluoromethyl cyclic ether compounds as substance P antagonists
DK1029456T3 (en) 1998-09-09 2005-12-05 Q P Corp Anti-emetic food
DE60012953T2 (en) * 1999-10-07 2005-08-18 Hisamitsu Pharmaceutical Co., Inc., Tosu 3-AMINO-2-PHENYLPIPERIDIN DERIVATIVES AS SUBSTANCE P ANTAGONISTS
US7728155B2 (en) 2003-10-24 2010-06-01 Wyeth Llc Dihydrobenzofuranyl alkanamines and methods for using same as cns agents
WO2013004766A1 (en) 2011-07-04 2013-01-10 Ferrari Giulio Nk-1 receptor antagonists for treating corneal neovascularisation
US20210015834A1 (en) 2018-02-26 2021-01-21 Ospedale San Raffaele S.R.L. Nk-1 antagonists for use in the treatment of ocular pain
EP4117673A1 (en) 2020-03-11 2023-01-18 Ospedale San Raffaele S.r.l. Treatment of stem cell deficiency

Citations (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO1994013663A1 (en) * 1992-12-10 1994-06-23 Pfizer Inc. Aminomethylene substituted non-aromatic heterocycles and use as substance p antagonists
US5393762A (en) * 1993-06-04 1995-02-28 Pfizer Inc. Pharmaceutical agents for treatment of emesis

Family Cites Families (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5232929A (en) * 1990-11-28 1993-08-03 Pfizer Inc. 3-aminopiperidine derivatives and related nitrogen containing heterocycles and pharmaceutical compositions and use
CA2106200C (en) * 1991-03-26 1996-11-19 Terry J. Rosen Stereoselective preparation of substituted piperidines

Patent Citations (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO1994013663A1 (en) * 1992-12-10 1994-06-23 Pfizer Inc. Aminomethylene substituted non-aromatic heterocycles and use as substance p antagonists
US5393762A (en) * 1993-06-04 1995-02-28 Pfizer Inc. Pharmaceutical agents for treatment of emesis

Non-Patent Citations (2)

* Cited by examiner, † Cited by third party
Title
Mishina et al. Preparation of imidazolybenzene compounds and use thereof as medicines CA 123:83361, 1995. *
Naylor et al. Preparation of benzofuran derivatives as tachykinin antagonists CA 123:339709, 1995. *

Cited By (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US20030152626A1 (en) * 1998-05-26 2003-08-14 Steffen Lang New pharmaceutical compositions
US6949257B2 (en) 1998-05-26 2005-09-27 Novartis Ag Pharmaceutical compositions
US6239147B1 (en) * 1999-05-21 2001-05-29 Pfizer Inc 1-trifluoromethyl-4-hydroxy-7-piperidinyl-aminomethylchroman derivatives
US7235257B1 (en) * 1999-12-14 2007-06-26 Rohto Pharmaceutical Co., Ltd. Drugs for relieving hemicrania comprising 1-menthol and essential oils
US20070218143A1 (en) * 2006-03-20 2007-09-20 Chong Mok T M Topical preparation

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